1628191-50-3

Basic information

• Product Name: N,N‐dimethyl‐2‐oxo‐2‐(4‐(trifluoromethyl)phenyl)acetamide
• Synonyms: N,N‐dimethyl‐2‐oxo‐2‐(4‐(trifluoromethyl)phenyl)acetamide
• CAS NO: 1628191-50-3
• Molecular Weight: 245.201
• Mol File: 1628191-50-3.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: N,N‐dimethyl‐2‐oxo‐2‐(4‐(trifluoromethyl)phenyl)acetamide(CAS DataBase Reference)
• NIST Chemistry Reference: N,N‐dimethyl‐2‐oxo‐2‐(4‐(trifluoromethyl)phenyl)acetamide(1628191-50-3)
• EPA Substance Registry System: N,N‐dimethyl‐2‐oxo‐2‐(4‐(trifluoromethyl)phenyl)acetamide(1628191-50-3)

Safety Data

• Hazardous Substances Data: 1628191-50-3(Hazardous Substances Data)

Upstream product

• 96604-36-3 1-(4-trifluoromethylphenyl)-3-(dimethylamino)-prop-2-en-1-one 
• 680-31-9 N,N,N,N,N,N-hexamethylphosphoric triamide 
• 709-63-7 1-(4-trifluoromethylphenyl)ethanone 
• 111991-14-1 2-(4-trifluoromethylphenyl)oxirane 
• 68-12-2 N,N-dimethyl-formamide 

Relevant articles and documents

Copper-Mediated Synthesis of Aryl α-Keto Amides from Epoxide Derivatives

A novel Cu II -mediated synthesis of aryl α-keto amides from epoxide derivatives is reported. This transformation was conducted by using O 2 as a green oxidant that meets the requirements of sustainable chemistry.

Copper-catalyzed, hypervalent iodine mediated C=C bond activation of enaminones for the synthesis of α-keto amides

An unprecedented C=C bond cleavage of enaminones has been realized by means of copper catalysis in the presence of hypervalent iodine (PhI(OAc)2). The cascade transformation based on this bond cleavage leads to the synthesis of various α-keto amides. Isotope labeling experiments suggest that water has acted as a source of oxygen atoms during the generation of the new carbonyl group.