86298-24-0

Basic information

• Product Name: N-phenyl-1H-benzo[d][1,2,3]triazole-1-carboxamide
• Synonyms: N-phenyl-1H-benzo[d][1,2,3]triazole-1-carboxamide
• CAS NO: 86298-24-0
• Molecular Weight: 238.249
• Mol File: 86298-24-0.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: N-phenyl-1H-benzo[d][1,2,3]triazole-1-carboxamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-phenyl-1H-benzo[d][1,2,3]triazole-1-carboxamide(86298-24-0)
• EPA Substance Registry System: N-phenyl-1H-benzo[d][1,2,3]triazole-1-carboxamide(86298-24-0)

Safety Data

• Hazardous Substances Data: 86298-24-0(Hazardous Substances Data)

Upstream product

• 68985-05-7 1,1′-carbonylbis-benzotriazole 
• 62-53-3 aniline 
• 95-14-7 1,2,3-Benzotriazole 
• 582-61-6 benzoyl azide 
• 98-88-4 benzoyl chloride 
• 495-18-1 Benzohydroxamic acid 
• 65-85-0 benzoic acid 
• 57709-64-5 N¹-(2-aminophenyl)-N²-phenylurea 
• 103-71-9 phenyl isocyanate 

Downstream Products

• 4300-33-8 N-(4-methylphenyl)-N'-phenylurea 
• 3083-88-3 N-butyl-N'-phenylurea 
• 1538-74-5 N-phenyl-carbamic acid butyl ester 
• 101-99-5 N-carboethoxyaniline 
• 621-12-5 1,4-diphenylsemicarbazide 
• 19102-24-0 2-methyl-4-phenyl semicarbazide 
• 73096-22-7 1-phenylcarbamoyl-L-proline 
• 84860-35-5 (S)-(phenylcarbamoyl)-N-valine 
• 438056-19-0 (S)-2-(3-phenylureido)-3-(indol-3-yl)propionic acid 
• 92033-74-4 N-((phenylamino)carbonyl)leucine 
• 93850-62-5 (S)-2-(3-phenylureido)-propionic acid 
• 33558-02-0 L-3-phenyl-2-(3-phenyl-ureido)-propionic acid 
• 4559-92-6 N-phenylmorpholine-4-carboxamide 

Relevant articles and documents

Simple, novel synthesis for 1-carbamoyl-lH-benzotriazole and some of its analogs

1-Carbamoyl-1H-benzotriazole (benzotriazole-1-carboxamide, 2a), an effective carbamoyl chloride substitute, and a range of its analogs can be synthesized in good yields in two very simple steps from 1,2-diaminobenzene. The facile preparation of the interm

One-pot preparation of carbamoyl benzotriazoles and their applications in the preparation of ureas, hydrazinecarboxamides and carbamic esters

Carbamoyl benzotriazoles were conveniently synthesized in one-pot from carboxylic acids, diphenyl phosphorazidate (DPPA) and 1H-benzotriazole (BtH). The reactivity and applications of carbamoyl benzotriazoles were also explored. Carbamoyl benzotriazoles react smoothly with amino acids, hydrazines and alcohols, thus providing facile access to the corresponding ureas, hydrazinecarboxamides and carbamic esters, respectively, in good to excellent yields.

Trapping! of isocyanates with benzotriazole in situ - Preparation of carbamoyl benzotriazoles as an isocyanate alternative via curtius rearrangement

N-Aryl and N-alkenyl carbamoyl benzotriazoles were prepared in good to excellent yields from acyl azides and benzotriazole via Curtius rearrangement, while N-alkylcarbamoyl benzotriazoles were formed from N-alkanoyl benzotriazoles and sodium azide in one