119020-88-1

Basic information

• Product Name: N-(1-benzotriazol-1-yl-1-phenylmethyl)acetamide
• Synonyms: N-(1-benzotriazol-1-yl-1-phenylmethyl)acetamide
• CAS NO: 119020-88-1
• Molecular Weight: 266.302
• Mol File: 119020-88-1.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: N-(1-benzotriazol-1-yl-1-phenylmethyl)acetamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(1-benzotriazol-1-yl-1-phenylmethyl)acetamide(119020-88-1)
• EPA Substance Registry System: N-(1-benzotriazol-1-yl-1-phenylmethyl)acetamide(119020-88-1)

Safety Data

• Hazardous Substances Data: 119020-88-1(Hazardous Substances Data)

Upstream product

• 117067-47-7 N-(1-Benzotriazol-1-yl-butyl)-benzamide 
• 117067-46-6 N-(1-Benzotriazol-1-yl-2-methyl-propyl)-benzamide 
• 119020-86-9 N-(1-Benzotriazol-1-yl-hexyl)-benzamide 
• 60-35-5 acetamide 
• 95-14-7 1,2,3-Benzotriazole 
• 100-52-7 benzaldehyde 

Downstream Products

• 195969-43-8 N-(2-acetyl-3-oxo-1-phenyl-butyl)-acetamide 
• 92653-04-8 ethyl 2-(acetamido(phenyl)-methyl)-3-oxobutanoate 
• 93025-98-0 (α-acetylamino-benzyl)-malonic acid diethyl ester 
• 1080529-60-7 N-[(1-benzyl-1H-indol-3-yl)(phenyl)methyl]acetamide 
• 1080529-56-1 N-[phenyl(2-phenyl-1H-indol-3-yl)methyl]acetamide 
• 1080529-63-0 N-[(5-bromo-1H-indol-3-yl)(phenyl)methyl]acetamide 
• 1080529-53-8 N-[(2-methyl-1H-indol-3-yl)(phenyl)methyl]acetamide 
• 1080529-45-8 N-[(1H-indol-3-yl)(phenyl)methyl]acetamide 
• 117067-47-7 N-(1-Benzotriazol-1-yl-butyl)-benzamide 
• 117067-46-6 N-(1-Benzotriazol-1-yl-2-methyl-propyl)-benzamide 
• 117067-49-9 N-[1-benzotriazol-1-yl-1-(4-methylphenyl)methyl]acetamide 
• 119020-86-9 N-(1-Benzotriazol-1-yl-hexyl)-benzamide 
• 588-46-5 N-(phenylmethyl)acetamide 
• 313471-97-5 N-(2-ethyl-inden-1-yl)acetamide 

Relevant articles and documents

N-(α-Amidoalkyl)benzotriazole-mediated synthesis of β′-amido β-diketones: a general synthetic protocol for N-[β-(3,5-di and 1,3,5-trisubstituted pyrazol-4-yl)alkyl] amides

Various β′-amido-β-diketones were first synthesized with N-(α-amidoalkyl)benzotriazole-mediated amidoalkylation of 1,3-diketones in moderate yields. These intermediates undergo rapid condensation with hydrazines to give the corresponding N-[β-(3,5-di and

N-(1-Benzotriazol-1-ylalkyl)amides, Versatile α-Amidoalkylation Reagents. 1. α-Amidoalkylation of CH Acids

N-(1-Benzotriazol-1-ylalkyl)amides 2, easily prepared from an amide and an aldehyde with benzotriazole, react smoothly with CH acids under mild conditions to give the α-amidoalkylation products in good yields.Benzotriazole aminals also react with CH acids in the presence of methyl iodide.