312944-36-8

Basic information

• Product Name: (1H-benzo[d][1,2,3]triazol-1-yl)(3-(trifluoromethyl)phenyl)methanone
• Synonyms: (1H-benzo[d][1,2,3]triazol-1-yl)(3-(trifluoromethyl)phenyl)methanone
• CAS NO: 312944-36-8
• Molecular Weight: 291.232
• Mol File: 312944-36-8.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: (1H-benzo[d][1,2,3]triazol-1-yl)(3-(trifluoromethyl)phenyl)methanone(CAS DataBase Reference)
• NIST Chemistry Reference: (1H-benzo[d][1,2,3]triazol-1-yl)(3-(trifluoromethyl)phenyl)methanone(312944-36-8)
• EPA Substance Registry System: (1H-benzo[d][1,2,3]triazol-1-yl)(3-(trifluoromethyl)phenyl)methanone(312944-36-8)

Safety Data

• Hazardous Substances Data: 312944-36-8(Hazardous Substances Data)

Upstream product

• 454-92-2 3-(trifluoromethyl)benzoic acid 
• 95-14-7 1,2,3-Benzotriazole 

Downstream Products

• 403-96-3 1,3-bis(m-α,α,α-trifluorotolyl)urea 
• 2354-93-0 ethyl (3-(trifluoromethyl)phenyl)carbamate 

Relevant articles and documents

An efficient one-pot synthesis of: N, N ′-disubstituted ureas and carbamates from N -acylbenzotriazoles

A facile and high-yielding one-pot synthesis of carbamates and N,N′-disubstituted symmetrical ureas from N-acylbenzotriazoles has been devised. It is believed that, the intermediate acyl-azide undergo Curtius rearrangement and in different solvents gives different products i.e. carbamates in alcohols and N,N′-disubstituted symmetrical urea in THF.

An Improved N-Acylation of 1 H-Benzotriazole Using 2,2′-Dipyridyl?-di?-sulfide and Triphenylphosphine

A novel path has been developed for the conversion of carboxylic acids into the corresponding N-acylbenzotriazoles by using 2,2′-dipyridyl disulfide/PPh 3 in anhydrous dichloromethane in the presence of 1 H-benzotriazole. Mild reaction conditio

A new methodology for the synthesis of N-acylbenzotriazoles

A facile and economic path for an easy access of diverse N-acylbenzotriazoles from carboxylic acid has been devised using NBS/PPh3 in anhydrous dichloromethane. High yield of product was obtained at room temperature in one hour reaction time under mild reaction conditions.