65720-27-6

Basic information

• Product Name: 1H-1,2,4-Triazole-3-carboxamide, 1-[4-chloro-2-(2-chlorobenzoyl)phenyl]-5-[[[(dimethylamino)acetyl]amino ]methyl]-N,N-dimethyl-
• CAS NO: 65720-27-6
• Molecular Formula: C23H24Cl2N6O3
• Molecular Weight: 503.388
• Mol File: 65720-27-6.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 1H-1,2,4-Triazole-3-carboxamide, 1-[4-chloro-2-(2-chlorobenzoyl)phenyl]-5-[[[(dimethylamino)acetyl]amino ]methyl]-N,N-dimethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-1,2,4-Triazole-3-carboxamide, 1-[4-chloro-2-(2-chlorobenzoyl)phenyl]-5-[[[(dimethylamino)acetyl]amino ]methyl]-N,N-dimethyl-(65720-27-6)
• EPA Substance Registry System: 1H-1,2,4-Triazole-3-carboxamide, 1-[4-chloro-2-(2-chlorobenzoyl)phenyl]-5-[[[(dimethylamino)acetyl]amino ]methyl]-N,N-dimethyl-(65720-27-6)

Safety Data

• Hazardous Substances Data: 65720-27-6(Hazardous Substances Data)

Upstream product

• 65699-27-6 2',5-dichloro-2-(3-dimethylcarbamoyl-5-chloroacetylaminomethyl-1H-1,2,4-triazol-1-yl)benzophenone 
• 124-40-3 dimethyl amine 
• 50330-59-1 8-chloro-6-(2-chloro-phenyl)-4H-benzo[f][1,2,4]triazolo[1,5-a][1,4]diazepine-2-carboxylic acid dimethylamide 
• 2958-36-3 (2-amino-5-chloro-phenyl)-(2-chloro-phenyl)-methanone 
• 65699-21-0 2',5-dichloro-2-(3-dimethylcarbamoyl-5-benzyloxycarbonylaminomethyl-1H-1,2,4-triazol-1-yl)benzophenone 
• 65699-26-5 2',5-dichloro-2-(3-dimethylcarbamoyl-5-aminomethyl-1H-1,2,4-triazol-1-yl)benzophenone hydrobromide 
• 85815-52-7 N,N-dimethyl 2-chloro-2-(2-(2-chlorobenzoyl)-5-chlorophenylazo)acetoacetamide 
• 65698-98-8 C₁₇H₁₅Cl₂N₃O₃ 
• 65698-99-9 N,N-dimethyl 2-amino-2-(2-(2-chlorobenzoyl)-5-chlorophenylazo)acetamide 

Relevant articles and documents

Synthesis and biological activity of (3,5-disubstituted-1H-1,2,4-triazol-1-yl)benzophenone derivatives (1)

The synthesis of (5-acylaminomethyl-3-carbamoyl-1H-1,2,4-triazol-1-yl)benzophenone derivatives is described. Acylation of the key intermediate, 1-benzoylphenylazo-1-aminoacetamide followed by cyclization in the presence of acid afforded 1H-1,2,4-triazole derivates. These compounds were evaluated for their central nervous system (CNS) activity. Some of these compounds exhibited high activities in anti-pentylene tetrazole and rotarod test in mice orally administered.