864736-87-8

Usage

Type of compound

Chlorinated aromatic compound

Structural components

Three chlorine atoms
One benzene ring
A trifluoroprop-1-en-2-yl group

Usage

Building block in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals
Manufacturing of polymers, resins, and other industrial products

Environmental and health concerns

Toxicity
Persistence in the environment

Handling and disposal

Proper handling and disposal to minimize impact on human health and the environment

Upstream product

• 64634-61-3 1,2,3-trichloro-5-iodobenzene 
• 139954-92-0 Trifluoroisopropenylzinc 
• 87-61-6 1,2,3-trichlorobenzene 
• 1514-82-5 2-bromo-3,3,3-trifluoropropene 
• 862248-93-9 (3,4,5-trichlorophenyl)boronic acid 
• 942069-95-6 3,4,5-trichlorophenylboronic acid pinacol ester 

Downstream Products

• 1092486-03-7 5-[4,5-dihydro-5-(3,4,5-trichlorophenyl)-5-(trifluoromethyl)-3-isoxazolyl]-2-fluorobenzonitrile 
• 1132700-90-3 3-(3-chloro-4-methylphenyl)-5-(3,4,5-trichlorophenyl)-5-trifluoromethyl-4,5-dihydroisoxazole 
• 1338473-74-7 N-(2-bromo-5-(5-(3,4,5-trichlorophenyl)-5-(trifluoromethyl)-4,5-dihydroisoxazol-3-yl)benzyl)acetamide 
• 1338473-70-3 N-{2-chloro-5-[5-(3,4,5-trichlorophenyl)-5-(trifluoromethyl)-4,5-dihydroisoxazol-3-yl]benzyl}acetamide 
• 1338473-88-3 1-{2-chloro-5-[5-(3,4,5-trichlorophenyl)-5-(trifluoromethyl)-4,5-dihydroisoxazol-3-yl]phenyl}methanamine 
• 1338473-96-3 (2-bromo-5-(5-(3,4,5-trichlorophenyl)-5-(trifluoromethyl)-4,5-dihydroisoxazol-3-yl)phenyl)methanamine 
• 1338473-87-2 tert-butyl 2-chloro-5-(5-(3,4,5-trichlorophenyl)-5-(trifluoromethyl)-4,5-dihydroisoxazol-3-yl)benzylcarbamate 
• 1338473-76-9 tert-butyl {5-[5-(3,4,5-trichlorophenyl)-5-(trifluoromethyl)-4,5-dihydroisoxazol-3-yl]-2-fluorobenzyl}-carbamate 
• 1338473-95-2 tert-butyl 2-bromo-5-(5-(3,4,5-trichlorophenyl)-5-(trifluoromethyl)-4,5-dihydroisoxazol-3-yl)benzylcarbamate 
• 1437779-62-8 4-fluoro-3,3-dimethyl-5-(5-(3,4,5-trichlorophenyl)-5-(trifluoromethyl)-4,5-dihydro isoxazol-3-yl)benzo[c][1,2]oxaborol-1(3H)-ol 
• 1437779-64-0 6-fluoro-3,3-dimethyl-5-(5-(3,4,5-trichlorophenyl)-5-(trifluoromethyl)-4,5-dihydroisoxazol-3-yl)benzo[c][1,2]oxaborol-1(3H)-ol 
• 1437779-82-2 (S)-3,3-dimethyl-5-(5-(3,4,5-trichlorophenyl)-5-(trifluoromethyl)-4,5-dihydroisoxazol-3-yl)benzo[c][1,2]oxaborol-1(3H)-ol 
• 1437779-39-9 (R)-3,3-dimethyl-5-(5-(3,4,5-trichlorophenyl)-5-(trifluoromethyl)-4,5-dihydroisoxazol-3-yl)benzo[c][1,2]oxaborol-1(3H)-ol 
• 1437779-28-6 3,3-dimethyl-5-(5-(3,4,5-trichlorophenyl)-5-(trifluoromethyl)-4,5-dihydroisoxazol-3-yl)benzo[c][1,2]oxaborol-1(3H)-ol 

Relevant academic research and scientific papers

BORON-CONTAINING SMALL MOLECULES

This invention provides novel compounds, methods of using the compounds, and pharmaceutical compositions containing the compounds.

BORON-CONTAINING SMALL MOLECULES

This invention provides novel compounds, methods of using the compounds, and pharmaceutical formulations comprising the compounds.

4-Azolylphenyl isoxazoline insecticides acting at the GABA gated chloride channel

Isoxazoline insecticides have been shown to be potent blockers of insect GABA receptors with excellent activity on a broad pest range, including Lepidoptera and Hemiptera. Herein we report on the synthesis, biological activity and mode-of-action for a class of 4-heterocyclic aryl isoxazoline insecticides.

SUBSTITUTED ISOXAZOLINE DERIVATIVES

This invention recites substituted isoxazoline derivatives of Formula (1) or a veterinarily acceptable salt thereof, with parasiticidal activity, compositions thereof, and their use as a parasiticide in animals or birds where R1a, R1b/sup

SUBSTITUTED ISOXAZOLINE COMPOUND AND PEST CONTROL AGENT

There is provided a novel pest control agent, particularly an insecticide or miticide. A substituted isoxazoline compound of General Formula (1): where A1, A2 and A3 independently are CH or N, etc., X1, X2

3-CYANO-4-TRIAZOLYL PHENYLISOXAZOLINE INVERTEBRATE PEST CONTROL AGENTS

Disclosed are compounds of Formula 1, N-oxides, and salts thereof; Formula (I) wherein R1 is F, Cl, Br, cyano, CF3, OCF2H, OCF3 or OCH2CF3; R2 is H, F, Cl, Br, CH3, cy