112281-77-3

Usage

Uses

Used in Agricultural Industry:
Tetraconazole is used as a fungicide for controlling pests in various crops, such as apple and strawberries. It helps in preventing the growth and spread of fungal diseases, ensuring a healthy and productive harvest.
TETRACONAZOLE is used as an agricultural fungicide for controlling powdery mildew, brown rust, Septoria, and Rhyncosporium on cereals. This helps in maintaining the quality and quantity of cereal crops, which are a staple food source for many.
TETRACONAZOLE is used as a fungicide for managing powdery mildew and scab on apples. By controlling these fungal infections, it helps in preserving the fruit's quality and preventing economic losses due to crop damage.
TETRACONAZOLE is used as a fungicide for treating powdery mildew on vines and cucumbers. This ensures the health of the plants and contributes to a better yield of these crops.
TETRACONAZOLE is used as a fungicide for managing powdery mildew and beet leaf spot on sugar beet. This helps in maintaining the health of the sugar beet plants and improving the overall sugar production.
TETRACONAZOLE is used as a fungicide for controlling powdery mildew and rust on vegetables. This helps in protecting the vegetables from fungal infections, ensuring a healthy and safe food supply for consumers.

Metabolic pathway

There is little published information available.

Degradation

Tetraconazole decomposes at 240 °C without boiling. It is stable in dilute solutions at pH 5 to 9 and, in water, it is stable to sunlight (PM).

InChI:InChI=1/C13H11Cl2F4N3O/c14-9-1-2-10(11(15)3-9)8(4-22-7-20-6-21-22)5-23-13(18,19)12(16)17/h1-3,6-8,12H,4-5H2

Upstream product

• 116-14-3 polytetrafluoroethylene 

Downstream Products

• 131320-41-7 (+)-tetraconazole 
• 131320-41-7 (-)-tetraconazole 
• 131320-41-7 (-)-S-1-[2-(2,4-dichlorophenyl)-3-(1,1,2,2-tetrafluoroethoxy)propyl]-1H-1,2,4-triazole 
• 131320-41-7 (+)-R-1-[2-(2,4-dichlorophenyl)-3-(1,1,2,2-tetrafluoroethoxy)propyl]-1H-1,2,4-triazole 

Relevant academic research and scientific papers

PROCESS FOR THE PREPARATION OF TETRACONAZOLE

The present invention relates to a new process for the preparation of Tetraconazole or one of its optically active isomers by means of the fluorination of 2- (2,4- dichlorophenyl) -3- (1H-1, 2, 4-triazol-1-yl) propan-1-ol.

Synergistic Fungidical Active Substance Combinations

The present invention relates to novel active substance combinations which contain spiroxamine, which is known, a known azole and a known carboxamide and which are very suitable for controlling undesired phytopathogenic fungi.

Pyrazolyl benzyl ether derivatives containing a fluoromethoxyimino group and use thereof as pesticides

The invention relates to novel pyrazolyl benzyl ethers, to a plurality of processes for their preparation and to their use for controlling harmful organisms.

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.

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.

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.

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.

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.

Enzymatic preparation of optically active fungicide intermediates in aqueous and in organic media

Pure stereoisomers of two new triazole and morpholine fungicides have been prepared starting from enzymatically synthesized chiral alcohol intermediates.Two resolution strategies compared are: lipase-catalyzed hydrolysis of corresponding acetates in water and lipase-catalyzed transesterification of alcohols in organic solvents.The antifungal activity of optically pure enantiomers of the synthesized fungicides investigated in vitro and in vivo against a variety of fungi, show an activity ratio (R-form/S-form) up to 400.

Fungicidal azolyl-derivatives

Disclosed are compounds having the formula: STR1 wherein: m=0, 1; n=0, 1; Z=CH, N; R1 is selected from chlorine, bromine, fluorine, CF3, phenyl, C1 -C2 -alkoxy, C1 -C2 -haloalkoxy, alkylthi