1384290-43-0

Basic information

• Product Name: 2-diazo-N-(2,4-dimethylphenyl)-3-oxobutanamide
• Synonyms: 2-diazo-N-(2,4-dimethylphenyl)-3-oxobutanamide
• CAS NO: 1384290-43-0
• Molecular Weight: 231.254
• Mol File: 1384290-43-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2-diazo-N-(2,4-dimethylphenyl)-3-oxobutanamide(CAS DataBase Reference)
• NIST Chemistry Reference: 2-diazo-N-(2,4-dimethylphenyl)-3-oxobutanamide(1384290-43-0)
• EPA Substance Registry System: 2-diazo-N-(2,4-dimethylphenyl)-3-oxobutanamide(1384290-43-0)

Safety Data

• Hazardous Substances Data: 1384290-43-0(Hazardous Substances Data)

Upstream product

• 97-36-9 m-acetoacetoxylidide 

Downstream Products

• 1384290-63-4 1,1'-(hexane-1,6-diyl)bis(N-(2,4-dimethylphenyl)-5-methyl-1H-1,2,3-triazole-4-carb-oxamide) 
• 1384290-60-1 N-(2,4-dimethylphenyl)-5-methyl-1H-1,2,3-triazole-4-carboxamide 
• 866871-73-0 N-(2,4-dimethylphenyl)-5-methyl-1-phenyl-1H-1,2,3-triazole-4-carboxamide 
• 1586765-32-3 C₁₄H₁₇NO₄ 
• 1421851-94-6 N²,N⁴-bis(2,4-dimethylphenyl)-2,5-dimethyl-3-oxo-1-phenyl-2,3-dihydro-1H-pyrrole-2,4-dicarboxamide 

Relevant articles and documents

Intramolecular hydrogen bonding-assisted cyclocondensation of α-diazoketones with various amines: A strategy for highly efficient Wolff 1,2,3-triazole synthesis

A catalytic and highly efficient Wolff's cyclocondensation of α-diazoketones with aromatic and aliphatic amines has been realized for the first time by utilizing the strategy of an intramolecular hydrogen bonding-activating carbonyl group. This approach successfully solved the challenging problem of poor condensation efficiency in Wolff 1,2,3-triazole synthesis, and constitutes a powerful method for the synthesis of highly functionalized 1,2,3-triazoles. The Royal Society of Chemistry 2012.