1189122-34-6

Basic information

• Product Name: (Z)-N-(4-oxo-4-(p-tolyl)but-2-en-2-yl)acetamide
• Synonyms: (Z)-N-(4-oxo-4-(p-tolyl)but-2-en-2-yl)acetamide
• CAS NO: 1189122-34-6
• Molecular Weight: 217.268
• Mol File: 1189122-34-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (Z)-N-(4-oxo-4-(p-tolyl)but-2-en-2-yl)acetamide(CAS DataBase Reference)
• NIST Chemistry Reference: (Z)-N-(4-oxo-4-(p-tolyl)but-2-en-2-yl)acetamide(1189122-34-6)
• EPA Substance Registry System: (Z)-N-(4-oxo-4-(p-tolyl)but-2-en-2-yl)acetamide(1189122-34-6)

Safety Data

• Hazardous Substances Data: 1189122-34-6(Hazardous Substances Data)

Upstream product

• 122-00-9 para-methylacetophenone 
• 60-35-5 acetamide 
• 4023-79-4 1-(4-methylphenyl)butan-1,3-dione 

Downstream Products

• 1260522-23-3 N-(4-oxo-4-p-tolylbutan-2-yl)acetamide 

Relevant articles and documents

Hypervalent iodane mediated reactions of: N -acetyl enamines for the synthesis of oxazoles and imidazoles

A hypervalent iodane reagent used for the intramolecular cyclization of N-acetyl enamines and intermolecular cyclocondensation of enamines and nitriles was investigated. The reaction was performed under mild conditions and gave oxazoles and imidazoles, respectively, in moderate to excellent yields. This transformation exhibits good reactivity, selectivity and functional group tolerance. The selectivity of the intra- or intermolecular reaction is dependent on the structure of N-acetyl enamines.

Rhodium-catalyzed enantioselective and diastereoselective hydrogenation of β-ketoenamides: Efficient access to anti 1,3-amino alcohols

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