6656-72-0

Usage

Uses

Used in Pharmaceutical Industry:
Benzenamine, 2,6-dichloro-3-(trifluoromethyl)is used as an intermediate in the synthesis of various pharmaceuticals. Its unique chemical structure allows for the development of new drugs with specific therapeutic properties.
Used in Agrochemical Industry:
Benzenamine, 2,6-dichloro-3-(trifluoromethyl)is also utilized in the production of agrochemicals, where it serves as a key intermediate in the synthesis of pesticides and other agricultural chemicals. Its strong reactivity enables the creation of effective and targeted agrochemicals.
Used in Dye Industry:
Benzenamine, 2,6-dichloro-3-(trifluoromethyl)is used as a building block in the synthesis of various dyes. Its distinct chemical properties contribute to the development of dyes with specific color characteristics and application properties.
It is crucial to handle Benzenamine, 2,6-dichloro-3-(trifluoromethyl)with care, as it can pose risks to human health and the environment if not properly managed. Its strong reactivity and potential hazards necessitate proper safety measures during its production, use, and disposal.

InChI:InChI=1/C7H4Cl2F3N/c8-4-2-1-3(7(10,11)12)5(9)6(4)13/h1-2H,13H2

Upstream product

• 2926-29-6 Langlois reagent 
• 608-31-1 2,6-Dichloroaniline 
• 121-50-6 3-amino-4-chlorobenzotrifluoride 
• 203915-49-5 1,3-dichloro-2-nitro-4-(trifluoromethyl)benzene 

Downstream Products

• 6690-41-1 2-(2,6-Dichloro-3-trifluoromethyl-phenylamino)-benzoic acid 

Relevant academic research and scientific papers

PYRIMIDINE UREA DERIVATIVES AS KINASE INHIBITORS

The invention relates to compounds of formula (I) wherein the substituents X1, R1, R2, R3 and R4 have the meaning as set forth and explained in the description of the invention, to processes for the preparation of these compounds, pharmaceutical compositions containing same, the use thereof optionally in combination with one or more other pharmaceutically active compounds for the therapy of a disease which responds to an inhibition of protein kinase activity, and a method for the treatment of such a disease.

Trifluoromethylation of aromatic compounds with sodium trifluoromethanesulfinate under oxidative conditions

Radical trifluoromethylation occurs without Cu(II) but cations are involved with Cu(II). Electron-rich aromatic compounds are triluforomethylated with sodium trifluoromethanesulfinate and t-butyl hydroperoxide. Monotrifluoromethylation predominates in the presence of catalytic amounts of Cu(II) triflate whereas mono- and bis-trifluoromethylated aromatics are obtained in almost equal quantities in the absence of Cu(II).

Substituted 1,2,4-triazolo[1,5-a]pyrimidine-2-sulfonamides, compositions containing them, and their utility as herbicides

Novel substituted triazolo[1,5-a]pyrimidine-2-sulfonamides, e.g., 5,7-dimethyl-N-(2,6-dichlorophenyl)-1,2,4-triazolo[1,5-a]pyrimidine-2-sulfonamide and their agriculturally acceptable salts are prepared. These compounds and compositions containing them are useful for the control of unwanted vegetation. Novel substituted triazolo[1,5-a]pyrimidine-2-sulfonyl chlorides and substituted anilines and their use as intermediates are also described.

Novel substituted 1,2,4-triazolo[1,5-a]pyrimidine-2-sulfonamides and compositions and method for inhibiting pollen formation in corn

Novel compounds, e.g., 5,7-dimethyl-N-(2,6-dichlorolphenyl)-1,2,4-triazolo[1,5-a]pyrimidine-2-sulfonamide and their compositions and use in the control of weeds and in the suppression of nitrification of ammonium nitrogen in soil. Other novel compounds and their compositions and use in the inhibition of bolting in sugar beets. Other novel compounds and their compositions and use as plant gametocides.