332021-26-8

Basic information

• Product Name: (1H-benzo[d][1,2,3]triazol-1-yl)(2-iodophenyl)methanone
• Synonyms: (1H-benzo[d][1,2,3]triazol-1-yl)(2-iodophenyl)methanone
• CAS NO: 332021-26-8
• Molecular Weight: 349.131
• Mol File: 332021-26-8.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: (1H-benzo[d][1,2,3]triazol-1-yl)(2-iodophenyl)methanone(CAS DataBase Reference)
• NIST Chemistry Reference: (1H-benzo[d][1,2,3]triazol-1-yl)(2-iodophenyl)methanone(332021-26-8)
• EPA Substance Registry System: (1H-benzo[d][1,2,3]triazol-1-yl)(2-iodophenyl)methanone(332021-26-8)

Safety Data

• Hazardous Substances Data: 332021-26-8(Hazardous Substances Data)

Upstream product

• 95-14-7 1,2,3-Benzotriazole 
• 88-67-5 2-Iodobenzoic acid 

Downstream Products

• 13114-94-8 1-(2-iodophenyl)-3-phenylurea 
• 99512-79-5 C₁₃H₉IOS 
• 54149-07-4 2-Iodo-thiobenzoic acid S-p-tolyl ester 
• 1242149-27-4 C₁₃H₈ClIOS 

Relevant articles and documents

Facile synthesis of N-acylbenzotriazoles from carboxylic acids mediated by 2,4,6-trichloro-1,3,5-triazine and triethylamine

Abstract A facile, efficient, and economic method toward N-acylbenzotriazoles was reported using 2,4,6-trichloro-1,3,5-triazine in combination with triethylamine as a carboxylic acid activator. Through reacting 1H-benzotriazole with the generated triacylated triazine intermediate, a series of N-acylbenzotriazoles could be rapidly prepared in high yields without column chromatography.

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