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Iminoacetic acid amides and their use as pest control agents
PCT No. PCT/EP96/04345 Sec. 371 Date Apr. 15, 1998 Sec. 102(e) Date Apr. 15, 1998 PCT Filed Oct. 7, 1996 PCT Pub. No. WO97/14673 PCT Pub. Date Apr. 24, 1997Iminoacetamides of the formula (I) in which A represents a single bond or optionally substituted alkylene, Q represents oxygen or sulphur, R1 represents respectively optionally substituted cycloalkyl, cycloalkenyl, aryl or heterocyclyl, R2 represents respectively optionally substituted alkyl, alkenyl, alkinyl, cycloalkyl, cycloalkenyl, aryl or heterocyclyl, R3 represents hydrogen or respectively optionally substituted alkyl, alkenyl, alkinyl or cycloalkyl, R4 represents respectively optionally substituted cycloalkyl, cycloalkenyl, aryl or heterocyclcyl a process for their preparation, pesticidal compositions containing them, and their use for controlling pests.
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(2008/06/13)

Microbicidal benzotriazoles
Novel benzotriazoles of the formula STR1 in which R, X1, X2, X3, X4 and Y have the meanings given in the description, and their acid addition salts and metal salt complexes, a process for the preparation of these substances and their use as microbicides in crop protection and in material protection.
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(2008/06/13)

Halogen alkenyl azolyl microbicides
Novel halogenoalkenyl-azolyl derivatives of the formula STR1 in which R1 represents optionally substituted alkyl, optionally substituted alkenyl, optionally substituted cycloalkyl, optionally substituted aryl or represents optionally substituted heteroaryl, R2 represents alkyl, halogenoalkyl, 1-hydroxyalkyl, 2-hydroxyalkyl, 1-hydroxyhalogenalkyl, 1-alkenyl or 2-alkenyl, X1 represents fluorine, chlorine, bromine or iodine, X2 represents fluorine, chlorine, bromine or iodine, and Y represents nitrogen or a CH group, and addition products thereof with acids or metal salts are very active as microbicides in plant protection and in the protection of materials.
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(2008/06/13)

Substituted biphenyl oxazolines
The invention relates to new substituted biphenyloxazolines of the formula (I) STR1 in which R1 represents C1 -C6 -halogenoalkylthio and R2 represents hydrogen, or R1 and R2 together with the carbon atoms to which they are bonded form a halogen-substituted 5- or 6-membered heterocyclic ring, X represents hydrogen, halogen, C1 -C6 -alkyl or C1 -C6 -alkoxy, and m represents 0, 1 or 2, to processes for their preparation, to new intermediates, and to the use of the substituted biphenyloxazolines for combating animal pests, with the exception of the compound of the formula STR2
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(2008/06/13)

Acylated 5-aminopyrazoles and the use thereof to combat animal parasites
The present invention relates to new acylated 5-aminopyrazoles of the formula (I) STR1 in which R1, R2, R3, R4 and R5 have the meaning given in the description, to processes for their preparation and to their use as pesticides.
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(2008/06/13)

Substituted tetrahydro-5-nitro-pyrimidines
The present invention relates to novel substituted in that one tetrahydro-5-nitro-pyrimidine of the formula (I), according to claim 1, STR1 in which n, R1, R2 have the meaning given in the description, to a process for its preparation and to its use for combating animal pests, especially insects, arachnids and nematodes, which are encountered in agricultural, in forestry, in the protection of stored products and of materials and, in the hygiene sector.
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(2008/06/13)

Method for controlling phytopathogenic fungi
A method for controlling phytopathogenic fungi comprises applying a selected fungicidally active N-acetonylbenzamide compound and a second fungicidally active compound selected from the group consisting of manganese-zinc ethylenebis(dithiocarbamate), manganese ethylenebis(dithiocarbamate), zinc ammoniate ethylenebis(dithiocarbamate), zinc ethylenebis(dithiocarbamate), 2-cyano-N-((ethylamino)carbonyl)-2-(methoxyimino)acetamide, and (E,Z) 4-(3-(4-chlorophenyl)-3-(3,4-dimethoxyphenyl)acryloyl)morpholine to plant seed, to plant foliage or to a plant growth medium and provides higher fungicidal activity than separate use of the same compounds.
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(2008/06/13)

Diaryl derivatives and their use as crop protection agents
Diaryl derivatives of the general formula I STR1 where A is =CHOR1, =CHSR1, =CHR1, =CHCl or =NOR1, B is OR2, SR2 or NR2 R3 and Het is a mono-, di- or trinuclear aromatic five- or six-membered heterocyclic structure which is unsubstituted or substituted by R, R1, R2, R3, R4, R5 are identical or different and each is hydrogen or alkyl, and U, V, W are identical or different and each is halogen, alkyl or alkoxy, and fungicides containing these compounds.
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(2008/06/13)

Synergistic fungicidal compositions of N-acetonyl-benzamides
A method for controlling phytopathogenic fungi comprises applying a selected fungicidally active N-acetonylbenzamide compound and a second fungicidally active compound selected from the group consisting of manganese-zinc ethylenebis(dithiocarbamate), manganese ethylenebis(dithiocarbamate), zinc ammoniate ethylenebis(dithiocarbamate), zinc ethylenebis(dithiocarbamate), 2-cyano-N-((ethylamino)carbonyl)-2-(methoxhyimino)acetamide, and (E,Z) 4-(3-(4-chlorophenyl)-3-(3,4-dimethoxyphenyl)acryloyl)morpholine to plant seed, to plant foliage or to a plant growth medium and provides higher fungicidal activity than separate use of the same compounds.
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(2008/06/13)

β-substituted cinnamic acid derivative
β-Substituted cinnamic acid derivatives of the formula 1, STR1 where R1 is substituted or unsubstituted alkyl, alkenyl, alkynyl, cycloalkyl or cycloalkenyl, and R1 can also be chlorine or bromine, --X-- is --O--, --S--, STR2 m is 0 or 1, --Y is --OR4, --O--N=CR5 R6, --NR7 R8, --NR7 R8, --N(OR9)R10 or SR11, where the abovementioned substitutes R2 to R11 are substituted or unsubstituted alkyl, alkenyl, alkynyl, cycloalkyl or cycloalkenyl, and R2, R3 and R5 to R11 can be hydrogen and Z, U, V, W are defined in the specification.
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(2008/06/13)

α-arylacrylic acid derivatives, their preparation and use for controlling pests and fungi
α-Arylacrylic acid derivatives of the formula I STR1 where the substituents have the following meanings: X C, N Y CR4, N, O, S Z CR5, N, O, S n 0 to 4 R1 hydrogen, nitro, cyano, halogen; alkyl, alkoxy, halogenated alkyl, halogenated alkoxy or alkylthio, or, when n is 2, 3 or 4, two adjacent substituents R1 may together denote a 1,3-butadien-1,4-diyl group which may be substituted; R2 alkyl; halogenated alkyl, halogen, cyano, nitro, alkoxycarbonyl, dimethylamino, R2 additionally denotes hydrogen; R3 hydrogen; substituted or unsubstituted alkyl; a substituted or unsubstituted cyclic structure, which may contain, in addition to carbon atoms, one to three heteroatoms; or a substituted or unsubstituted aromatic system, which may contain, in addition to carbon atoms, one to four nitrogen atoms and one to three heteroatoms; R4, R5 hydogen, alkyl; halogenated alKyl, halogen, cyano, nitro, dimethylamino, alkoxycarbonyl and pesticides and fungicidal agents containing these compounds.
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(2008/06/13)

Fungicidal composition for seed dressing
The present invention relates to a fungicidal composition intended for the protection of the multiplication products of cultivated plants, containing: (a) 2-(4-chlorobenzylidene)-5,5-dimethyl-1-(1H-1,2,4-triazol-1-ylmethyl)-1-cyclopentanol; (b) one or more fungicides suitable for the protection of the said multiplication products, optionally one or more insecticides, (c), an agriculturally acceptable inert vehicle and an agriculturally acceptable surfactant. The invention also relates to a method for protecting the multiplication products of plants against fungal diseases using these compositions.
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(2008/06/13)

Anilide derivatives and their use for combating botrytis
The use of nicotinic anilide derivatives of the general formula STR1 where the substituents have the following meanings: R1 halogen, methyl, trifluoromethyl, methoxy, methylthio, methylsulfinyl, methylsulfonyl R2 unsubstituted or halogen-substituted alkyl, unsubsituted or halogen-substituted alkenyl, alkynyl, unsubstituted or halogen-substituted alkoxy, unsubstituted or halogen-substituted alkenyloxy, alkynyloxy, cycloalkyl, cycloalkenyl, cycloalkyloxy, cycloalkenloxy for combating Botrytis, and nicotinic anilides of the formula I.
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(2008/06/13)

4-(4-tert-butylphenyl) cyclohexylamines, and fungicides containing same
4-4(tert-butylphenyl)-cyclohexylamines and quaternary ammonium salts thereof of the formulae STR1 where R1 is hydrogen, alkyl or alkenyl, R2 is alkyl, haloalkyl, hydroxyalkyl, cycloalkyl, alkylcycloalkyl, bicycloalkyl, alkenyl, unsubstituted or mon- to trisubstituted phenyl, or unsubstituted or mono- to trisubstituted phenylalkyl, X? is a plant-tolerated acid anion, and their plant-tolerated acid addition salts, and fungicides containing these compounds.
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(2008/06/13)

α-Hydroxyazolylethyloxiranes and fungicides containing these compounds
α-Hydroxyazolylethyloxiranes of the general formula I STR1 where R1 and R2 are each alkyl, cycloalkyl, cycloalkenyl, phenyl, biphenyl, naphthyl or pyridyl, these radicals being unsubstituted or substituted, and X is CH or N, their plant-tolerated acid addition salts and metal complexes, and fungicides containing these compounds.
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(2008/06/13)

Unsaturated cyclohexylacetic acid derivatives, and crop-protection agents containing same
Unsaturated cyclohexylacetic acid derivatives of the formula I STR1 where U is=NOCH3, =CHOCH3, =CH2, =CH--CH3, =CH--CH2 --CH3, =N--NH--CH3 or =CH--S--CH3, n is from 0 to 10, A is hydrogen or substituted or unsubstituted alkyl, cycloalkyl, aryl or hetaryl, and X is a single bond when n is 0, and oxygen, sulfur or a single bond when n is not 0, and the plant-compatible acid addition products and base addition products thereof, and fungicides and insecticides containing these compounds.
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(2008/06/13)

Sulfur-containing acrylic esters and fungicides containing them
Acrylic esters of the formula STR1 where R1 and R2 are hydrogen or alkyl, X is S, SO or SO2, R3 is phenyl, naphthyl or phenanthrenyl, these radicals being unsubstituted or substituted, with the exception of compounds in which R3 is phenyl, 3-chlorophenyl, 4-chlorophenyl, 2,4-dichlorophenyl or methylphenyl, and fungicides containing these compounds.
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(2008/06/13)

Sulfur-containing oxime ethers and fungicides containing them
Oxime ether derivatives of the formula STR1 where R1 and R2 are each hydrogen or alkyl, X is S, SO or SO2, R3 is hydrogen, cycloalkyl, phenyl, naphthyl, quinolinyl or phenanthrenyl, these radicals being unsubstituted or substituted, Y is alkylene, alkenylene or alkynylene, and m is 0 or 1.
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(2008/06/13)

Phenylalkylamines and fungicides containing these
Phenylalkylamines of the formula STR1 where n is 5, 6, 7, 8 or 9, m is 1, 2 or 3, R1 is methyl, halogen, substituted or unsubstituted aryl or substituted or unsubstituted phenoxy, and, when m is 2, two adjacent radicals R1 together denote the radical STR2 X is oxygen, except when R1 is methyl, or the radical STR3 R4 is isopropyl, tert-butyl or substituted or unsubstituted phenyl and R5 is H or OH, R2 and R3 are each hydrogen and, when X is oxygen, R2 and R3 additionally denote methyl or ethyl, and their plant-tolerated salts, and fungicides containing these compounds.
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(2008/06/13)

Azolylmethyloxiranes and fungicides containing them
Azolylmethyloxiranes of the general formula I STR1 where R1, R2 and R3 are substituted or unsubstituted alkyl, benzyl, naphthyl, biphenyl, dioxanyl, phenyl, tetrahydropyranyl, tetrahydrofuranyl, norbornyl, C3 -C12 -cycloalkyl or C3 -C12 -cycloalkenyl, and X is CH or N, and plant-tolerated acid addition salts and metal complexes thereof, and fungicides containing these compounds.
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(2008/06/13)

Methyl α-arylacrylates substituted by a heterocyclic radical and their use
Methyl α-arylacrylates substituted by a heterocyclic radical and having the general formula STR1 where R is alkyl, alkenyl, haloalkyl, cycloalkyl, alkoxy, alkylcarbonyl, alkoxycarbonyl, halogen or aryl, the aromatic ring being unsubstituted or substituted, Het is a five-membered heteroaromatic ring which is unsubstituted or substituted and has from one to three heteroatoms, and A is ethenylene, ethylene, methyleneoxy or methylenethio, and fungicides and pesticides containing these compounds.
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(2008/06/13)

2-Anilinocyanopyridines having fungicidal properties
2-Anilinocyanopyridines of the formula STR1 where X is NO2, CN, halogen, SO2 -alkyl, alkyl, cycloalkyl, haloalkyl, alkoxy, or phenoxy or phenylthio which is unsubstituted or substituted in the phenyl, m is an integer from 1 to 3, R1 is hydrogen, halogen, alkoxy, haloalkyl, haloalkoxy, or phenoxy or phenylthio which is unsubstituted or substituted in the phenyl, R2 and R3 are hydrogen, NO2, halogen, CN, alkyl, SO2 -alkyl, haloalkyl, SO2 NR5 R6, haloalkoxy, COOR5 or CONR5 R6, R4 is hydrogen, COOR7, CONR5 R6, CHO, COR7, SO2 R7, C3 -C6 -alkenyl or C3 -C6 -alkynyl, and salts of these 2-anilinocyanopyridines of the formula I in which R4 is hydrogen with plant-tolerated cations, and fungicides containing these compounds.
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(2008/06/13)

Azolymethylcycloalkyloxiranes and therir use as crop protection agents
Azolylmethyloxiranes of the general formula I STR1 where A and B are cycloalkyl, tetrahydropyranyl, tetrahydrofuranyl, dioxanyl, norbornyl, cycloalkenyl or phenyl, each of these radicals being unsubstituted or substituted, with the proviso that A and B are not simultaneously phenyl, D is O, X is CH or N, and their plant-tolerated acid addition salts or metal complexes, and fungicides containing these compounds.
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(2008/06/13)

α-arylacrylates substituted by a heterocyclic radical, and fungicides which contain these compounds
α-Arylacrylates substituted by a heterocyclic radical and of the general formula I STR1 where R1 is alkoxy or alkylthio, R2 is alkyl, Het is pyridyl, pyridone, quinolyl, pyrimidinyl, pyrimidinone, the heterocyclic ring system being unsubstituted or substituted, A is carbonyloxy, oxygen or sulfur, and n is 0 or 1, and their plant-tolerated acid addition salts and metal complexes, and the N-oxides of the heterocyclic compounds, and fungicides containing these compounds.
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(2008/06/13)

Derivatives of 1-hydroxy-1,2,4-triazole and fungicides and growth regulators containing them
Compounds of the formula I STR1 where Ar is unsubstituted or substituted phenyl, pyridyl, thienyl or napthyl, R1 is hydrogen or CN, R2 is unsubstituted or substituted aryl, hetaryl, alkyl or cycloalkyl, or is unsubstituted or substituted alkenyl or alkynyl, x is CH2, O or S and n is 0 or 1, their plant-tolerated acid addition salts and metal complexes, and fungicides and growth regulators containing these compounds.
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(2008/06/13)

Azolylmethylallyl alcohols and fungicides containing these compounds
Azolylmethylallyl alcohols of the formula I STR1 where R1 and R2 are alkyl, naphthyl, biphenyl, cycloalkyl, cycloalkenyl or phenyl, these radicals being unsubstituted or substituted, X is CH or N, their plant-tolerated acid addition salts and metal complexes, and fungicides containing these compounds.
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(2008/06/13)

Ortho-substituted benzyl carboxylates and fungicides containing these compounds
Benzyl carboxylates of the formula STR1 where R1 is alkyl, R2 is hydrogen, alkyl or alkoxy, R3 is hydrogen, halogen, cyano, aryl or aryloxy, the aromatic ring being unsubstituted or substituted, or R3 is heteroaryl, adamantyl, fluorenyl or cycloalkyl or cycloalkenyl, the radicals being unsubstituted or substituted, X is saturated or unsaturated, substituted or unsubstituted alkylene, and n is 0 or 1, and fungicides containing these compounds.
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(2008/06/13)

1-halo-1-azolylpropenes and -methyloxiranes and fungicides containing these compounds
1-Halo-1-azolylpropenes and -methyloxiranes of the formula I STR1 where R1 and R2 are alkyl, cycloalkyl, cycloalkenyl, tetrahydropyranyl, norbornyl, pyridyl, naphthyl, biphenyl or phenyl, A is oxygen or a single bond, R3 is F, Cl or Br, X is CH or N, their plant-tolerated acid addition salts and metal complexes, and fungicides containing these compounds.
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(2008/06/13)

Acrylates and fungicides containing them
X is hydrogen, halogen, cyano, nitro, substituted or unsubstituted alkyl, substituted or unsubstituted alkoxy, substituted or unsubstituted haloalkyl, n is 1, 2, 3 or 4, Y is substituted or unsubstituted alkylene, alkenylene, alkynylene, O, S(O), unsubstituted or alkyl-substituted N, oxycarbonyl, carbonyloxy, carbonyloxyalkylene, oxycarbonylalkylene, oxyalkylene, thioalkylene, azo, carbonylamino, aminocarbonyl, STR2 methylenoxy or methylenethio and Z is hydrogen, alkyl, cycloalkyl, aryl, aralkyl, aralkenyl, aralkoxy, aryloxy, aryloxyalkyl, hetaryl, alkoxy, alkoxyalkyl, alkylthio, or haloalkyl, these radicals being unsubstituted or substituted by halogen, cyano, nitro, alkyl, alkenyl, haloalkenyl, alkoxy, haloalkyl, alkoxycarbonyl or unsubstituted or substituted phenyl, and fungicides containing these compounds.
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(2008/06/13)

Aminomethylphenols and fungicides containing these compounds
o-Aminomethylphenols of the formula STR1 where R1, R3 and R4 are hydrogen, fluorine, chlorine, bromine, alkyl, alkoxy or dimethylamino, R2 is hydrogen, chlorine, bromine, alkyl, alkenyl, alkoxyalkyl, cyclohexyl or phenyl, or R1 and R2, R2 and R3 or R3 and R4 form a carbocyclic, saturated or unsaturated five-membered or six-membered ring, and R is alkyl, and salts thereof, and fungicides containing these compounds.
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(2008/06/13)

Substituted imidazolylmethyloxiranes and substituted imidazolylpropenes, their preparation and fungicides containing them
Substituted imidazolylmethyloxiranes and substituted imidazolylpropenes of the general formula I STR1 where R1 and R2 are alkyl, cycloalkyl, cycloalkenyl, tetrahydropyranyl, norbornyl, pyridyl, naphthyl, biphenyl or phenyl, D is oxygen or a single bond, E is H, F, Cl or Br, X, Y and Z are hydrogen, halogen, nitro, cyano, alkyl, haloalkyl, alkoxy, unsubstituted or substituted amino, unsubstituted or substituted mercapto, acyl, alkoxycarbonyl, hydroxyalkyl or substituted or unsubstituted phenyl, and acid addition salts and metal complexes thereof tolerated by plants, processes for their manufacture, and fungicides containing them.
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(2008/06/13)

1-halo-azolylethane derivatives and fungicides containing them
1-Halo-1-azolylethane derivatives of the formula I STR1 where R1 and R2 are C1 -C8 -alkyl, phenyl, biphenyl, naphthyl, benzyl, C3 -C8 -cycloalkyl or C3 -C8 -cycloalkenyl, each of which is unsubstituted or substituted, n is an integer from 1 to 5, or 0, E is Cl or Br, and X is CH or N, their plant-tolerated acid addition salts and metal complexes, and fungicides containing these compounds.
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(2008/06/13)

Azolylmethylcyclopropanes and their use as crop protection agents
Azolylmethylcyclopropanes of the formula STR1 where R is alkyl, cycloalkyl, cycloalkenyl, tetrahydropyranyl, norbornyl, pyridyl, naphthyl, biphenyl or phenyl, and these radicals are substituted or unsubstituted, A is H, F, Cl or Br, and X is CH or N, their plant-tolerated acid addition salts and metal complexes, and fungicides and growth-regulating agents containing these compounds.
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(2008/06/13)

Ortho-substituted phenol ethers and fungicides which contain these compounds
Ortho-substituted phenol ethers of the general formula I STR1 where R1 is C1 -C4 -alkyl, C1 -C4 -alkoxy, C1 -C4 -alkylthio or amino which is unsubstituted or mono- or disubstituted by C1 -C4 -alkyl, R2 is C1 -C4 -alkyl, R3 is aryloxy, arylthio or arylalkoxy, the aromatic ring being unsubstituted or substituted by one or more of the following radicals: halogen, C1 -C6 -alkyl, C1 -C6 -alkoxy, C1 -C4 -alkylthio, C1 -C2 -haloalkyl, aryl, aryl-C1 -C2 -alkoxy, C1 -C4 -alkylcarbonyl, mono- or di-C1 -C4 -alkylsubstituted amino, cyano, nitro, X is CH or N, and Y is saturated or unsaturated C2 -C12 -alkylene, and fungicides containing these compounds.
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(2008/06/13)

4-substituted cyclohexylamine derivatives, fungicides containing these and a method of controlling fungi
4-trans-substituted cyclohexylamine derivatives of the formula STR1 where R1 is the group CR5 R6 R7, in which R5, R6 and R7 are hydrogen, unsubstituted or substituted alkyl, alkoxy, alkylthio or cycloalkyl, with the proviso that not more than one of the substituents R5, R6 and R7 may by hydrogen, or in which R6 and R7 together with the included carbon atom form a three-membered to six-membered carbocyclic aliphatic ring, R2 and R3 are hydrogen, alkyl, alkenyl or alkynyl or cycloalkyl or cycloalkenyl, which in turn may be substituted, with the proviso that the sum of the carbon atoms and hetero atoms (O, S and halogen) of R2 and R3 together is not less than 8, R4 is hydrogen, alkyl, cycloalkyl or alkoxy, and m is 1 to 4, and the bond is a single or a double bond, salts thereof, and their use as fungicides.
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(2008/06/13)

Oxime ethers, their preparation and fungicides containing these compounds
Oxime ethers of the general formula STR1 where R1 and R2 are hydrogen or alkyl, R3 is hydrogen, halogen, cyano, aryl or aryloxy, the aromatic ring being unsubstituted or substituted, or R3 is heteroaryl, adamantyl, fluorenyl or cycloalkyl or cycloalkenyl, these radicals being unsubstituted or substituted, X is saturated or unsaturated C1 -C12 -alkylene which is unsubstituted or substituted, and n is 0 or 1, and fungicides containing these compounds.
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(2008/06/13)

Azolylmethyloxiranes and fungicides containing these compounds
Azolylmethyloxiranes of the general formula I STR1 where R1 and R2 are substituted or unsubstituted alkyl, naphthyl, biphenyl, dioxanyl or phenyl, m and n are each an integer from 1 to 5 or 0, with the proviso that m+n is 1 or more, D is oxygen or a single bond, X is CH or N, and their plant-tolerated acid addition salts and metal complexes, and fungicides containing these compounds.
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(2008/06/13)

Fungicidal N-substituted 3-arylpyrrolidine derivatives
N-Substituted 3-arylpyrrolidine derivatives of the formula STR1 where R1 is 2,2-dimethylpropyl, 3,3-dimethylbutyl, 4,4-dimethylpentyl, 2,4,4-trimethylpentyl, 6-methylhept-2-yl, 3,5,5-trimethylhexyl, 6,10-dimethylundec-2-yl, 3-methylcyclohexyl, 3,3-dimethylcyclohexyl, 3,3,5-trimethylcyclohexyl, 3,3,5,5-tetramethylcyclohexyl, 4-methylcyclohexyl, 4-ethylcyclohexyl, 4-propylcyclohexyl, 4-isopropylcyclohexyl, 4-tert.-butylcyclohexyl, trans-4-tert.-butylcyclohexyl, 4(2-methylbut-2-yl)cyclohexyl, 4(2,4,4-trimethylpent-2-yl)-cyclohexyl, cyclododecanyl, C3 -C9 -trialkylsilyl-substituted C4 -C12 -cycloalkyl, 4-hydroxycyclohexyl, 4-hydroxy-3-methylcyclohexyl, 4-hydroxy-3,5-dimethylcyclohexyl, 4-hydroxy-3,3-dimethylcyclohexyl, 4-hydroxy-3,3,5-trimethylcyclohexyl, unsubstituted or hydroxy-, C1 -C9 -alkyl-, C1 -C5 -alkoxy- or C3 -C9 -trialkylsilyl-substituted C5 -C12 -cycloalkenyl, R1 is further bicycloalkyl, R1 is further 4-tert.-butyl-benzyl, 4-chlorobenzyl, 4-tert.-butoxybenzyl, 1,4-dioxaspiro[4,5]decan-8-yl, 5 to 7-membered heterocycloalkyl, 5 to 7-membered heterocycloalkylmethyl, R2 is alkyl, alkoxy or trialkylsilyl, R3 is alkyl, alkenyl, alkynyl or arylalkyl, X- is a plant-tolerated anion, n is 0 or 1, and plant-tolerated salts thereof, and fungicides containing these compounds.
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(2008/06/13)

Dihydrodibenzofuran derivatives and fungicides containing these compounds
Substituted benzofuran derivatives of the formula STR1 where R1, R2 and R3 are hydrogen, an alkali or alkaline earth metal, alkyl, aralkyl, alkanoyl, halogen-substituted alkanoyl, benzoyl or a radical R4 R5 R6 Si in which R4, R5 and R6 are alkyl, and fungicides containing these compounds.
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(2008/06/13)

2-Aminodecalin derivatives and their use
2-Aminodecalin derivatives of the formula I STR1 where R1, R2 and R3 are H or methyl, A is H, OH, O-alkylcarbonyl, O-benzoyl or O-CH3, R4 is H, cyclopropyl, alkyl, alkenyl, or alkynyl, R5 is alkyl, alkenyl or alkynyl which is substituted or unsubstituted, cycloalkyl or cycloalkenyl whic is substituted or unsubstituted, substituted phenylalkyl, substituted cycloalkyl-alkyl, substituted 5-membered heterocyclic ring, bicycloalkyl-alkyl or R4 and R5, together with the nitrogen atom, are a substituted or unsubstituted, saturated or unsaturated piperidine radical, their plant-tolerated salts and N-oxides, and fungicides containing these compounds.
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(2008/06/13)

Fungicidal cyclohexylamines
4-substituted cyclohexylamines of the formula STR1 where R is the group CR1 R2 R3, where R1, R2 and R3 are hydrogen, unsubstituted or substituted alkyl, alkoxy, alkylthio or cycloalkyl, with the proviso that at most one of the substituents R1, R2 and R3 is hydrogen, X is an alkylene group which, together with the N atom, forms a substituted or unsubstituted heterocyclic ring in which up to 2 carbon atoms may be replaced by O, N or S atoms, and salts thereof, and fungicides containing these compounds.
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(2008/06/13)

Guanidinium compounds and fungicides containing them
Guanidiniumdodecylbenzene sulfonates of the formula STR1 where R is the group --H, --CH3 or STR2 and X is 1, 2, 3 or 4, and fungicides containing these compounds.
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(2008/06/13)

Ortho-substituted benzyl carboxylates and fungicides which contain these compounds
Ortho-substituted benzyl carboxylates of the formula STR1 where R1 is alkoxy, alkylthio, halogen or amino, R2 is alkoxycarbonyl, cyano or CONH2, R3 l is hydrogen, halogen, cyano, aryl, aryloxy, a saturated or unsaturated heterocyclic radical, cycloalkyl, or substituted cyclopropyl, X is alkylene, and n is 0 or 1, and fungicides containing these compounds.
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(2008/06/13)

N,N'-disubstituted piperazines
N,N'-disubstituted piperazines of the general formula I STR1 where the group is unsaturated (=) or saturated (--) and the substituents R1, R2 and A have the following meanings: A is --, --CH=, --CH2 --, --CH2 --CH2 --, R1 is alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl, alkylcycloalkyl, cycloalkenylalkyl, alkylcycloalkenyl, bicycloalkyl, bicycloalkylalkyl or alkylbicycloalkyl, these radicals being unsubstituted or substituted by hydroxy, halogen, alkoxy or trialkylsilyl, R1 is further heterocycloalkyl with oxygen and/or sulfur, heterocycloalkylmethyl with oxygen and/or sulfur, alkyl-substituted heterocycloalkylmethyl with oxygen and/or sulfur, and R2 is alkyl, alkoxy, trimethylsilyl, cycloalkyl, alkylthio, and plant-physiologically tolerated salts thereof, and fungicides containing these compounds.
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(2008/06/13)

Fungicidal imidazolylmethyloxiranes
Imidazolylmethyloxiranes of the general formula I STR1 where R is phenyl, pyridyl, tetrahydropyranyl, norbornyl, C3 -C12 -cycloalkyl or C5 -C8 -cycloalkenyl, these radicals being unsubstituted or substituted, and their plant-tolerated acid addition salts and metal complexes, and fungicides containing these compounds.
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(2008/06/13)

Cyclic amines and fungicides containing them
Amines of the general formula I STR1 where n is an integer from 2 to 10, X is oxygen or sulfur, Z is oxygen or CH--R5, and R1, R2, R3, R4 and R5 are identical or different and are each hydrogen or alkyl, salts thereof, and fungicides containing these compounds.
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(2008/06/13)

Propylamines, and their use as fungicides
N-Arylpropyl-substituted secondary amines of the formula STR1 where R1 and R2 are each hydrogen, alkyl, cycloalkyl, haloalkyl, alkoxy, chlorine, bromine or fluorine, m is 0, 1 or 2, R3 and R4 are each hydrogen or alkyl, and R5 is alkyl, cycloalkyl, cycloalkenyl, cycloalkylalkyl, alkenyl or an unsubstituted or substituted phenyl or phenylalkyl radical or methylfuran and the dashed bonds may be hydrogenated, and their salts, and fungicides containing these compounds.
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(2008/06/13)

Acrylates and fungicides which contain these compounds
Acrylates of the general formula STR1 where R1 and R2 independently of one another are each C1 -C8 -alkyl, X is hydrogen, C1 -C4 -alkyl, halogen, C1 -C4 -alkoxy, haloalkyl, cyano or nitro, W is unsubstituted or alkyl-substituted, saturated or unsaturated C1 -C10 -alkylene, Y is hydrogen, alkyl, haloalkyl, alkoxyalkyl, cycloalkyl, aralkyl, aryl, aryloxy, halogen, an unsubstituted or substituted C4 H4 chain which is fused to the benzene radical, alkoxy, haloalkoxy, alkylthio, thiocyanato, cyano, NO2, STR2 where R' and R" independently of one another are each hydrogen, alkyl, alkoxy, alkylthio or cycloalkyl, or are phenyl which is unsubstituted or substituted by alkyl, halogen or alkoxy, m is 0 or 1, n is from 1 to 4 and Z is oxygen, sulfur, SO or SO2, and fungicides containing them.
-
(2008/06/13)

Pyridine-N-oxides and fungicidal compositions containing same and fungical use
Substituted pyridine-N-oxides of the formula STR1 where R1 is alkyl and R2 is phenyl or substituted phenyl, salts thereof which are physiologically tolerated by plants, and fungicides containing them.
-
(2008/06/13)

Diastereomeric triazolyl glycol ethers-fungicides and growth regulators
Diastereomers of the formula STR1 Where R1 is hydrogen, alkyl, alkenyl, alkynyl or benzyl, R2 is a alkyl or alkenyl, R3 is alkyl or benzyl, and the asymmetric centers of the molecular have (a) an RR or SS or (b) an RS or SR configuration, and a process for their preparation and fungicides containing the compounds.
-
(2008/06/13)

Chemical Properties

Appearance/Colour :off-white powder
Melting Point: 157ºC (decomposes)
Boiling Point: 308.2 °C at 760 mmHg
Flash Point:140.2 °C
Density: 1.74 g/cm3
Storage Temp.:2-8°C
Vapor Pressure: <1x l0-5 at 20 °C
Merck: 13,10220
BRN: 4165797
PSA: 88.24000
LogP: 0.60850

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Chemical Properties

Appearance/Colour :off-white powder

Melting Point: 157ºC (decomposes)

Boiling Point: 308.2 °C at 760 mmHg

Flash Point:140.2 °C

Density: 1.74 g/cm3

Storage Temp.:2-8°C

Vapor Pressure: <1x l0-5 at 20 °C

Merck: 13,10220

BRN: 4165797

PSA: 88.24000

LogP: 0.60850

Global suppliers and manufacturers of 12122-67-7total 78 suppliers on LookChem