106044-11-5

Usage

Derivative of

Benzenemethanol

Attached groups

Two chlorine atoms at 3 and 4 positions, trifluoromethyl group

Uses

Synthesis of pharmaceuticals and agrochemicals, production of organic compounds

Handling

Careful handling required due to potential health and environmental hazards

Upstream product

• 125733-43-9 1-(3,4-dichlorophenyl)-2,2,2-trifluoroethan-1-one 
• 81290-20-2 (trifluoromethyl)trimethylsilane 
• 6287-38-3 3,4-dichlorobenzaldehyde 

Downstream Products

• 125733-43-9 1-(3,4-dichlorophenyl)-2,2,2-trifluoroethan-1-one 

Relevant academic research and scientific papers

Metal-free defluorinative arylation of trifluoromethyl alkenes: Via photoredox catalysis

Literature methods to access gem-difluoroalkenes are largely limited to harsh, organometallic-based methods, and known photoredox-mediated processes are not amenable to aryl radical addition to trifluoromethyl alkenes. A metal-free, functional group-tolerant method for the preparation of benzylic gem-difluoroalkenes is described. Halogen atom abstraction from (hetero)aryl halides generates aryl radicals that undergo a defluorinative arylation of α-trifluoromethyl alkenes, tolerating electronically disparate aryl radicals and α-trifluoromethyl alkenes.

Pesticidal compositions and processes related thereto

This document discloses molecules having the following formula (“Formula One”): and processes associated therewith.

PESTICIDAL COMPOSITIONS AND PROCESSES RELATED THERETO

This disclosure relates to the field of molecules having pesticidal utility against pests in Phyla Nematoda, Arthropoda, and/or Mollusca, processes to produce such molecules and intermediates used in such processes, compositions containing such molecules, and processes of using such molecules against such pests. These molecules may be used, for example, as nematicides, acaricides, insecticides, miticides, and/or molluscicides. This document discloses molecules having the following formula (“Formula One”).

PESTICIDAL COMPOSITIONS AND PROCESSES RELATED THERETO

This document discloses molecules having the following formula ("Formula One"): and processes associated therewith.

PESTICIDAL COMPOSITIONS AND PROCESSES RELATED THERETO

This document discloses molecules having the following formula (“Formula One”): and processes associated therewith.

PESTICIDAL COMPOSITIONS AND PROCESSES RELATED THERETO

This document discloses molecules having the following formula (“Formula One”): and processes associated therewith.

PESTICIDAL COMPOSITIONS AND PROCESSES RELATED THERETO

This document discloses molecules having the following formula ("Formula One") and processes associated therewith.

PESTICIDAL COMPOSITIONS AND PROCESSES RELATED THERETO

This document discloses molecules having the following formula (“Formula One”): and processes associated therewith.

N-[(alpha-perhaloalkylbenzyloxy)pyridyl]-N'-benzoylurea insecticides

N-[(Alpha-perhaloalkylbenzyloxy)pyridyl]-N'-benzoylurea compounds of the following structural formula are useful insecticides: STR1 in which RA is selected from the group consisting of -hydrogen, -halogen, -lower alkyl, -lower alkoxy, -benzyl,