1382223-55-3

Basic information

• Product Name: N-(4-cyanophenyl)-2-oxo-2-(3,4,5-trimethoxyphenyl)acetamide
• Synonyms: N-(4-cyanophenyl)-2-oxo-2-(3,4,5-trimethoxyphenyl)acetamide
• CAS NO: 1382223-55-3
• Molecular Weight: 340.335
• Mol File: 1382223-55-3.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: N-(4-cyanophenyl)-2-oxo-2-(3,4,5-trimethoxyphenyl)acetamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(4-cyanophenyl)-2-oxo-2-(3,4,5-trimethoxyphenyl)acetamide(1382223-55-3)
• EPA Substance Registry System: N-(4-cyanophenyl)-2-oxo-2-(3,4,5-trimethoxyphenyl)acetamide(1382223-55-3)

Safety Data

• Hazardous Substances Data: 1382223-55-3(Hazardous Substances Data)

Upstream product

• 150114-69-5 2-oxo-2-(3,4,5-trimethoxyphenyl)acetaldehyde 
• 873-74-5 4-Aminobenzonitrile 
• 87428-53-3 3,4,5-trimethoxy-α-hydroxyacetophenone 

Relevant articles and documents

IronO-Catalyzed Domino Aerobic Alcohol Oxidation/Oxidative Cross-Dehydrogenative Coupling for the Synthesis of α-Keto Amides

An ironO-catalyzed (TEMPO = 2,2,6,6-tetramethyl-1-piperidinyloxy), aerobic process was developed to synthesize α-keto amides. This reaction proceeds through a domino alcohol oxidation/oxidative cross-dehydrogenative coupling sequence, uses 2-hydroxyacetophenones and amines as the starting materials, and takes place under molecular oxygen, which makes the transformation highly efficient, practical, and environmentally friendly.