782-70-7

Basic information

• Product Name: N-ISOPROPYL-3-(TRIFLUOROMETHYL)BENZENECARBOXAMIDE
• Synonyms: N-ISOPROPYL-3-(TRIFLUOROMETHYL)BENZENECARBOXAMIDE;N-(propan-2-yl)-3-(trifluoromethyl)benzamide
• CAS NO: 782-70-7
• Molecular Formula: C₁₁H₁₂F₃NO
• Molecular Weight: 231.21
• Mol File: 782-70-7.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: N-ISOPROPYL-3-(TRIFLUOROMETHYL)BENZENECARBOXAMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: N-ISOPROPYL-3-(TRIFLUOROMETHYL)BENZENECARBOXAMIDE(782-70-7)
• EPA Substance Registry System: N-ISOPROPYL-3-(TRIFLUOROMETHYL)BENZENECARBOXAMIDE(782-70-7)

Safety Data

• Hazardous Substances Data: 782-70-7(Hazardous Substances Data)

Upstream product

• 2251-65-2 3-(Trifluoromethyl)benzoyl chloride 
• 75-31-0 isopropylamine 

Downstream Products

• 454-89-7 3-Trifluoromethylbenzaldehyde 
• 1611477-41-8 C₁₁H₁₁ClF₃N 

Relevant articles and documents

Photocatalysis in Aqueous Micellar Media Enables Divergent C-H Arylation and N-Dealkylation of Benzamides

Photocatalysis in aqueous micellar media has recently opened wide avenues to activate strong carbon-halide bonds. So far, however, it has mainly explored strongly reducing conditions, restricting the available chemical space to radical or anionic reactivity. Here, we demonstrate a controllable, photocatalytic strategy that channels the reaction of chlorinated benzamides via either a radical or a cationic pathway, enabling a chemodivergent C-H arylation or N-dealkylation. The catalytic system operates under mild conditions with methylene blue as a photocatalyst and blue LEDs as the light source. Factors determining the reactivity of substrates, their selectivity, and preliminary mechanistic studies are presented.

METHOD FOR THE CATALYTIC REDUCTION OF ACID CHLORIDES AND IMIDOYL CHLORIDES

The present application relates to methods for the catalytic reduction of acid chlorides and/or imidoyl chlorides. The methods comprise reacting the acid chloride or imidoyl chloride with a silane reducing agent in the presence of a catalyst such as [Cp(Pri3P)Ru(NCMe)2]+[PF6]?.