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Articles about 116255-48-2Total 45 be found

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SUBSTITUTED SPIROCYCLIC KETOENOLS
The present invention relates to novel substituted spirocyclic ketoenols of the formula (I) in which W, X, Y, Z, A, B, D and G are as defined in the disclosure, to a plurality of processes for their preparation and to their use as pesticides, microbicides and herbicides.
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(2008/06/13)

Glyoxyl acid amides, method for producing them and their use for controlling harmful organisms
The invention relates to novel gloyoxylic acid amides, to a process for their preparation and to their use for controlling harmful organisms.
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(2008/06/13)

Use of oxabicyclo[2.2.1]heptane derivatives as pesticidal agents
7-oxabicyclo[2.2.1]heptane derivatives of formula (I) in which X, R1, R2, R3 and R4 have the meanings set forth in the specification, are very suitable for controlling undesired microorganisms and animal pests. New 7-oxabicyclo[2.2.1]heptane derivatives of formula (Ia) in which X, R1, R2, R3 and R14 have the meanings set forth in the specification, and a process for the preparation of the new compounds.
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(2008/06/13)

Triazolopyrimidines
The invention relates to novel triazolopyrimidines of the formula 1wherein X represents halogen, Y represents a hydrogen atom or halogen, and R has the meanings given in the disclosure, to a process for the preparation of the new compounds, and to their use as microbicides.
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(2008/06/13)

Heterocyclic fluoroalkenyl thioethers and the use thereof as pesticides(III)
The present invention relates to novel heterocyclic fluoroalkenyl thioethers of the formula (I) in which X represents hydrogen, halogen or alkyl, m represents integers from 3 to 10, n represents 0, 1 or 2, Y represents sulphur or oxygen, R1 represents halogen, represents in each case optionally halogen-substituted alkyl, alkoxy, alkylthio, alkenyl, alkenyloxy, alkenylthio or alkylcarbonyl, represents optionally substituted cycloalkyl, represents optionally substituted aryl or represents optionally substituted heterocyclyl and R2 represents hydrogen, halogen, represents in each case optionally halogen-substituted alkyl, alkoxy, alkylthio, alkenyl, alkenyloxy, alkenylthio or alkylcarbonyl, represents optionally substituted cycloalkyl, represents optionally substituted aryl or represents optionally substituted heterocyclyl, ?except for compounds where R1=alkyl, Y=oxygen and X=hydrogen, and to processes for their preparation and to their use as pesticides.
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(2008/06/13)

Heterocyclic fluoroalkenyl thioethers and the use thereof as pesticides (I)
The present invention relates to novel heterocyclic fluoroalkenyl thioethers of the formula (I) in which X represents hydrogen, halogen or alkyl, m represents integers from 2 to 10, n represents 0, 1 or 2, Y represents unsubstituted or substituted methylene and p represents 1, 2 or 3. and to processes for their preparation and to their use as pesticides.
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(2008/06/13)

Substituted imide derivatives
The present invention relates to novel substituted imide derivatives of the general formula (I) in which R1 represents optionally substituted cycloalkyl, R2 represents optionally substituted alkyl or optionally substituted cycloalkyl, R3 represents alkyl, alkoxy, alkylthio, amino, alkylamino or dialkylamino and R4 represents cyano or nitro, and to processes for their preparation and to their use for controlling animal pests and as herbicides.
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(2008/06/13)

Substituted 3-thiocarbamoylpyrazoles
The invention relates to novel substituted 3-thiocarbamoylpyrazoles of general formula (I), wherein m, n, R1, R2, R3and Ar have the meanings cited in the description. The invention further relates to methods for the production and use thereof as pesticides.
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(2008/06/13)

Isothiazolecarboxylic acid derivatives and their use as microbicides
Novel isothiazolecarboxylic acid derivatives of the formula (I), in which A, Q, Z and k have the meanings mentioned in the specification, processes for the preparation of the new compounds and their use as microbicides.
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(2008/06/13)

Heterocylic fluoroalkenyl thioethers and the use thereof as pesticides (IV)
The present invention relates to novel heterocyclic fluoroalkenyl thioethers of the formula (I) in which m represents integers from 3 to 10, n represents 0, 1 or 2 and Het represents the following, in each case optionally substituted, groupings: and to processes for their preparation and to their use as pesticides.
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(2008/06/13)

Heterocyclic fluoroalkenyl thioethers (II)
The present invention relates to novel heterocyclic fluoroalkenyl thioethers of the formula (I) in which X represents hydrogen, halogen or alkyl, m represents integers from 3 to 10, n represents 0, 1 or 2, Het represents the groupings, where R1 represents hydrogen, mercapto, represents in each case optionally halogen-substituted alkyl, alkoxy, alkylthio, alkylsulphinyl, alkylsulphonyl or alkenyl, represents optionally substituted aryl or represents optionally substituted heterocyclyl, Y represents oxygen or sulphur, and R2 represents hydrogen, alkyl or optionally substituted aryl, and to processes for their preparation and to their use as pesticides.
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(2008/06/13)

Arylphenyl-substituted cyclic keto-enols
The present invention relates to novel arylphenyl-substituted cyclic ketoenols of the formula (I) in whichX represents halogen, alkyl, alkoxy, alkenyloxy, alkylthio, alkylsulphinyl, alkylsulphonyl, halogenoalkyl, halogeno-alkoxy, halogenoalkenyloxy, nitro, cyano or in each case optionally substituted phenyl, phenoxy, phenylthio, phenyl-alkoxy or phenylalkylthio,Y represents in each case optionally substituted cycloalkyl, aryl or hetaryl,Z represents hydrogen, halogen, alkyl, alkoxy, alkenyloxy, halogenoalkyl, halogenoalkoxy, halogenoalkenyloxy, nitro or cyano,CKE represents one of the groups ?in whichA, B, D, G and Q1 to Q6 are each as defined in the description, to a plurality of processes for their use as pesticides and herbicides.
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(2008/06/13)

3-phenyl-pyrones
Novel 3-phenyl-pyrones of the formula in which A, D, X and Y are each as defined in the description, a process for preparing these substances and their use as pesticides, fungicides and herbicides.
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(2008/06/13)

Utilization of 3-phenyl-pyrones for pest control
3-Phenyl-pyrones of the formula in which x represents pyrid-2-yl and Y represents fluorine, or x represents 4-fluoro-phenyl and Y represents chlorine, are highly suitable for use as pesticides, fungicides and herbicides.
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(2008/06/13)

Arylphenyl-substituted cyclic keto enols
The present invention relates to novel arylphenyl-substituted cyclic ketoenols, their preparation and the use of such ketoenols as pesticides and/or herbicides. The novel arylphenyl-substituted cyclic ketoenols are of the formula (I) in which CKE refers to the cyclic ketoenol and W, X, Y and Z are as defined in the specification.
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(2008/06/13)

Fungicidal benzoheterocyclyloxime
The invention relates to novel benzoheterocyclyloximes, to a process for their preparation and to their use as fungicides.
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(2008/06/13)

Methoximinomethyloxathiazines
The invention relates to novel methoximinomethyloxathiazines, to two processes for their preparation and to their use as pesticides.
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(2008/06/13)

Methoximinophenylacetic acid amides
The invention relates to novel methoximinophenylacetamides, to a process for their preparation and to their use as fungicides.
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(2008/06/13)

Azine used as fungicides
The invention relates to novel azines, to a process for their preparation and to their use as fungicides.
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(2008/06/13)

Use of 5-amino-pyrazol-derivatives for combating micro-organisms
A method of controlling a plant disease caused by a fungus comprising applying a 5-amino-pyrazole of the formula wherein, R1, R2, R3, R4, R5 and Y are as defined in the specification.
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(2008/06/13)

Pyrazole carboxanilide fungicide
Novel pyrazole-carboxanilides of the formula in which X, Y, m and n are each as defined in the description, a process for preparing these substances and their use for controlling undesirable microorganisms.
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(2008/06/13)

Substituted heterocyclic compounds and their use as fungicides
The invention relates to novel substituted heterocyclic compounds, to a plurality of processes for their preparation and to their use as fungicides, and to novel intermediates, to a plurality of processes for their preparation and to their use as fungicides.
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(2008/06/13)

Fungicide mixtures
A fungicidal mixture comprising a) an oxime ether of the formula I where the substituents have the following meanings: X is oxygen or amino (NH); Y is CH or N; Z is oxygen, sulfur, amino (NH) or C1-C4-alkylamino (N-alkyl); R′ is alkyl, haloalkyl, alkenyl, haloalkenyl, alkynyl, haloalkynyl, cycloalkylmethyl, or, if desired, substituted benzyl; a) an oxime ether of the formula I where the substituents have the following meanings: X is oxygen or amino (NH); Y is CH or N; Z is oxygen, sulfur, amino (NH) or C1-C4-alkylamino (N—C1-C4-alkyl); R′ is C1-C6-alkyl, C1-C6-haloalkyl, C3-C6-alkenyl, C2-C6-haloalkenyl, C3-C6-alkynyl, C3-C6-haloalkynyl, C3-C6-cycloalkylmethyl, or is benzyl which can be partially or fully halogenated and/or can have attached to it one to three of the following radicals: cyano, C1-C4-alkyl, C1-C4-haloalkyl, C1-C4-alkoxy, C1-C4-haloalkoxy and C1-C4-alkylthio; and at least one compound from groups b)-c): b.1) the oxime ether carboxylate of the formula IIa, b.2) the oxime ether carboxamide of the formula IIb, b.3) the methoxyacrylate of the formula IIc, c) one or more azole derivatives in a synergistically active amount.
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(2008/06/13)

Substituted aminosalicyclic acid amides with fungicidal effect and intermediate products for production thereof
The invention relates to novel substituted aminosalicylamides, to a plurality of processes for their preparation and to their use as fungicides, and also to novel intermediates and to a plurality of processes for their preparation.
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(2008/06/13)

Isothiazole carboxylic acid amides and the application thereof in order to protect plants
Novel isothiazolecarboxamides of the formula in which R is as defined in the description, a plurality of processes for preparing the novel compounds and their use for protecting plants against attack by undesirable microorganisms and animal pests.
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(2008/06/13)

Fungicidal alkoximinomethyldioxazine derivatives
The invention relates to alkoximinomethyldioxazine compounds and intermediates thereof, and to process for the preparation of the alkoximinomethyldioxazine compounds and intermediates thereof. The alkoximinomethyldioxazine compounds have the structure:
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(2008/06/13)

Fluoromethoximino compounds
The invention relates to novel fluoromethoximino compounds, to a process for their preparation and to their use as pesticides, and also to novel intermediates and to a plurality of processes for their preparation.
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(2008/06/13)

Fungicidal methoximinomethyldioxazines
The invention relates to novel methoximinomethyldioxazines, to a plurality of processes for their preparation and to their use as fungicides, and also to novel intermediates and to a process for their preparation.
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(2008/06/13)

Annulated azole derivatives useful as microbicidal agents
Novel fused azole derivatives of the formula in which R1, R2, A and G are as defined in the description, and also their acid addition salts and metal salt complexes, a plurality of processes for preparing these substances and their use as microbicides in crop protection and in the protection of materials.
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(2008/06/13)

Oxyranyle-triazoline thiones and their use as microbicides
Novel oxiranyl-triazolinethiones of the formula in which R1, R2and R3are each as defined in the description, a process for preparing the novel substances and their use as microbicides in crop protection and in the protection of materials.
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(2008/06/13)

Methoximinomethyloxadiazines
A compound of the formula (I) wherein Z represents a moiety selected from the group consisting of cycloalkyl having 3 to 7 carbon atoms in the cycloalkyl moiety or cycloalkylalkyl having 3 to 7 carbon atoms in the cycloalkyl moiety and 1 to 4 carbon atoms in the alkyl moiety, with said cycloalkyl or cycloalkylalkyl being in each case optionally mono- to pentasubstituted by halogen or alkyl; a heterocyclyl group selected from the group consisting of thienyl, pyridyl, furyl, thienylmethyl, pyridylmethyl or furylmethyl, each of which is optionally substituted by halogen, dialkylamino or alkyl having 1 to 4 carbon atoms; an aryl or arylalkyl having in each case 6 to 10 carbon atoms in the aryl moiety and 1 to 4 carbon atoms in Q represents oxygen or sulphur, X represents halogen and The compositions have microbicidal activity.
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(2008/06/13)

Sulfonyl benzazolones
Sulphonylbenzazolones of the formula in whichR1, R2, R3, R4, R5 and Q are each as defined in the description.a process for preparing these compounds and their use as microbicides in crop protection and in the protection of materials.
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(2008/06/13)

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)

Alkoxyacrylic acid thiol esters used as fungicides
PCT No. PCT/EP96/03436 Sec. 371 Date Feb. 10, 1998 Sec. 102(e) Date Feb. 10, 1998 PCT Filed Aug. 5, 1996 PCT Pub. No. WO97/07096 PCT Pub. Date Feb. 27, 1997The invention relates to novel alkoxyacrylic thiol esters, to a plurality of processes for their preparation and to their use as fungicides, and to novel intermediates and to a plurality of processes for their preparation.
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(2008/06/13)

Halogen pyrimidines and its use thereof as parasite abatement means
PCT No. PCT/EP97/00151 Sec. 371 Date Jul. 16, 1998 Sec. 102(e) Date Jul. 16, 1998 PCT Filed Jan. 15, 1997 PCT Pub. No. WO97/27189 PCT Pub. Date Jul. 31, 1997Compounds of the formula (I) in which A represents optionally substituted alkanediyl, R represents in each case optionally substituted cycloalkyl, aryl or benzo-fused heterocyclyl, E represents -CH= or nitrogen, Q represents oxygen, sulphur, -CH2-O-, a single bond, or a nitrogen atom which is optionally substituted by alkyl, and X represents halogen.
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(2008/06/13)

Use of sulfonyloxadiazolones as microbicides
PCT No. PCT/EP98/01988 Sec. 371 Date Oct. 14, 1999 Sec. 102(e) Date Oct. 14, 1999 PCT Filed Apr. 6, 1998 PCT Pub. No. WO98/47369 PCT Pub. Date Oct. 29, 1998Sulphonyloxadiazolones of the formula in which A represents a single bond or represents alkanediyl, alkenediyl, alkinediyl or a grouping -*O-CH2-, -*O-CH2-CH2-, -*CH2-O-, -*CH2-O-CH2-CH2-, -*CH2-S-, -*S-CH2-, or where the atom labelled by * is in each case attached to R1 and R3 represents hydrogen or alkyl, R1 represents hydrogen, optionally substituted cycloalkyl, optionally substituted cycloalkenyl, optionally substituted aryl or optionally substituted heterocyclyl and R2 represents in each case optionally substituted alkyl, alkenyl, dialkylamino, aryl or heterocyclyl, are highly suitable for controlling undesirable microorganisms in crop protection and in the protection of materials. Novel sulphonyloxadiazolones of the formula in which A and R1 are as defined above and R4 represents optionally substituted alkyl, optionally substituted alkenyl, dialkylamino, nitro-substituted phenyl which may also contain one or two further substituents, or represents optionally substituted heterocyclyl, but where R4 does not represent propyl if A represents a direct bond and R1 represents 2,4,5-trimethyl-phenyl, and a process for preparing these substances.
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(2008/06/13)

Sulphonyloxadiazolones
Novel sulphonyloxadiazolones of the formula STR1 in which A represents oxygen, sulphur, --SO--, --SO2 -- or STR2 where R3 represents hydrogen or alkyl, R1 represents optionally substituted cycloalkyl, optionally substituted cycloalkenyl or optionally substituted aryl and R2 represents in each case optionally substituted alkyl, alkenyl, dialkylamino or aryl a process for preparing these substances and their use as microbicides in crop protection and in the protection of materials.
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(2008/06/13)

1,3-dimethyl-5-fluoro-pyrazole-4-carboxamide derivatives, their preparation and their use as microbicides
PCT No. PCT/EP97/03692 Sec. 371 Date Jan. 20, 1999 Sec. 102(e) Date Jan. 20, 1999 PCT Filed Jul. 11, 1997 PCT Pub. No. WO98/03486 PCT Pub. Date Jan. 29, 1998The invention concerns 1,3-dimethyl-5-fluoro-pyrazole-4-carboxamides of formula (I) in which R stands for a group of formula(II) or (III), in which: R1 stands for alkyl, cycloalkyl, bicycloalkyl, optionally substituted aryl or optionally substituted aralkyl; m stands for integers from 0 to 3 or two vicinal R1 groups together stand for an alkylene chain with 3 or 4 carbon atoms; R2 stands for alkyl, cycloalkyl, bicycloalkyl, optionally substituted aryl or optionally substituted aralkyl; and n stands for integers from 0 to 3 or two vicinal R2 groups together stand for an alkylene chain with 3 or 4 carbon atoms. The invention further concerns a process for preparing the novel substances, and their use for combating undesirable micro-organisms for plant- and material-protection purposes.
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(2008/06/13)

Dihydrofuran carboxamides
The invention concerns novel dihydrofuran carboxamides of formula (I), STR1 in which R stands for groups of formulae (a), (b) or (c), STR2 in which R1, R2, R3, X, m, n and p have the meanings given in the description. The invention also concerns a process for preparing the novel substances, and their use for combating undesirable micro-organisms for plant- and material-protection purposes.
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(2008/06/13)

Sulphonyloxadiazolones and their use as microbicides
PCT No. PCT/EP98/01989 Sec. 371 Date Oct. 13, 1999 Sec. 102(e) Date Oct. 13, 1999 PCT Filed Apr. 6, 1998 PCT Pub. No. WO98/47897 PCT Pub. Date Oct. 29, 1998Novel sulphonyloxadiazolones of the formula in which A represents oxygen, sulphur, -SO-, -SO2- or where R3 represents hydrogen or alkyl, R1 represents optionally substituted cycloalkyl, optionally substituted cycloalkenyl or optionally substituted aryl and R2 represents optionally substituted heterocyclyl, a process for preparing these substances and their use as microbicides in crop protection and in the protection of materials.
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(2008/06/13)

Hydrazonoacetic acid amides and the use thereof as pesticides
The invention concerns hydrazonoacetic acid amides of general formula (I), a process for producing them, and the use of the said amides as pesticides. In the formula shown, the following meanings apply: A stands for a simple bond or optionally substituted alkylene; Q stands for oxygen or sulphur, R1 stands for optionally substituted cycloalkyl, cycloalkenyl, aryl or heterocyclyl; R2 stands for hydrogen or optionally substituted alkyl, cycloalkyl, cycloalkenyl, aryl or heterocyclyl; R3 and R4 are identical or different and each stand for hydrogen or optionally substituted alkyl or cycloalkyl; R2 and R3 together with the nitrogen atom to which they are bound form an optionally substituted heterocyclyl ring; R5 stands for optionally substituted cycloalkyl, cycloalkenyl, aryl or heterocyclyl.
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(2008/06/13)

Fungicidal mixtures
Fungicidal mixture, comprising a) an oxime ether carboxamide of the formula I STR1 where R is hydrogen or halogen and b) an azole derivative II selected from the group of the compounds II.1 to II.17 1-[(2RS,4RS;2RS,4SR)-4-bromo-2-(2,4-dichlorophenyl)-tetrahydrofuryl]-1H-1,2,4-triazole (II.1) 2-(4-chlorophenyl)-3-cyclopropyl-1-(1H-1,2,4-triazol-1-yl)butan-2-ol (II.2) (±)-4-chloro-4-[4-methyl-2-(1H-1,2,4-triazol-1-yl-methyl)-1,3-dioxolan-2-yl]phenyl 4-chlorophenyl ether (II.3) (E)-(R,S)-1-(2,4-dichlorophenyl)-4,4-dimethyl-2-(1H-1,2,4-triazol-1-yl)pent-1-en-3-ol (II.4) (Z)-2-(1H-1,2,4-triazol-1-ylmethyl)-2-(4-fluorophenyl)-3-(2-chlorophenyl)oxirane (II.5) 4-(4-chlorophenyl)-2-phenyl-2-(1H-1,2,4-triazolylmethyl)butyronitrile (II.6) 3-(2,4-dichlorophenyl)-6-fluoro-2-(1H-1,2,4-triazol-1-yl) quinazolin-4(3H)-one (II.7) bis(4-fluorophenyl)(methyl)(1H-1,2,4-triazol-1-yl-methyl)silane (II.8) (R,S)-2-(2,4-dichlorophenyl)-1-(1H-1,2,4-triazol-1-yl)hexan-2-ol (II.9) (1RS,5RS;1RS,5SR)-5-(4-chlorobenzyl)-2,2-dimenthyl-1-(1H-1,2,4-triazol-1-ylmethyl)cyclopentanol [sic] (II.10) N-propyl-N-[2-(2,4,6-trichlorophenoxy)ethyl]imidazole-1-carboxamide (II.11) (±)-1-[2-(2,4-dichlorophenyl)-4-propyl-1,3-dioxolan-2-ylmethyl]-1H-1,2,4-triazole (II.12) (R,S)-1-(4-chlorophenyl)-4,4-dimethyl-3-(1H-1,2,4-triazol-1-ylmethyl)pentan-3-ol (II.13) (±)-2-(2,4-dichlorophenyl)-3-(1H-1,2,4-triazolyl)-propyl 1,1,2,2-tetrafluoroethyl ether (II.14) and (E)-1-[1-[[4-chloro-2-(trifluoromethyl)phenyl]imino]-2-propoxyethyl]-1H-imidazole (II.15) (RS)-2,4'-difluoro-α-(1H-1,2,4-triazol-1-ylmethyl)-benzhydryl alcohol (II.16) 2-p-chlorophenyl-2-(1H-1,2,4-triazol-1-ylmethyl)-hexanenitrile (II.17) in a synergistically active amount.
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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 arylazadioxacyclo alkene fungicides
The invention relates to novel substituted arylazadioxacycloalkenes, a plurality of processes for their preparation and to their use as fungicides.
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(2008/06/13)

Microbicidal compositions based on dibromo-thiophene-carboxylic acid derivatives
New microbicidal compositions based on dibromo-thiophene-carboxylic acid derivatives which are known in some cases, of the formula STR1 in which R represents the groups --XR1, --NR2 R3, --NR4 OR5 or --NR4 --N(R5)2, where X represents oxygen or sulphur and R1, R2, R3, R4 and R5 have the meanings indicated in the description, and the use of these substances for controlling undesired microorganisms. New dibromo-thiophene-carboxylic acid derivatives of the formula STR2 in which R9 represents the groups --SR1, --OR10, STR3 in which R1, R4, R5, R10, R11, R12 and R13 have the meaning indicated in the description, and processes for the preparation of the substances of the formula (I-A).
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(2008/06/13)

Chemical Properties

Melting Point: 84oC
Boiling Point: 504.3oC at 760 mmHg
Flash Point:258.8oC
Density: 1.71g/cm3
Vapor Pressure: 2.69E-10mmHg at 25°C
Refractive Index: 1.6110 (estimate)
PKA: 2.75±0.10(Predicted)
BRN: 8393967
PSA: 39.94000
LogP: 3.66420

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116255-48-2

Articles about 116255-48-2Total 45 be found

Chemical Properties

Melting Point: 84oC

Boiling Point: 504.3oC at 760 mmHg

Flash Point:258.8oC

Density: 1.71g/cm3

Vapor Pressure: 2.69E-10mmHg at 25°C

Refractive Index: 1.6110 (estimate)

PKA: 2.75±0.10(Predicted)

BRN: 8393967

PSA: 39.94000

LogP: 3.66420

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