22326-34-7

Basic information

• Product Name: ethyl 2-amino-4-oxo-4-phenylbut-2-enoate
• Synonyms: ethyl 2-amino-4-oxo-4-phenylbut-2-enoate
• CAS NO: 22326-34-7
• Molecular Weight: 219.24
• Mol File: 22326-34-7.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: ethyl 2-amino-4-oxo-4-phenylbut-2-enoate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 2-amino-4-oxo-4-phenylbut-2-enoate(22326-34-7)
• EPA Substance Registry System: ethyl 2-amino-4-oxo-4-phenylbut-2-enoate(22326-34-7)

Safety Data

• Hazardous Substances Data: 22326-34-7(Hazardous Substances Data)

Upstream product

• 6296-54-4 ethyl 2,4-dioxo-4-phenylbutyrate 
• 94-02-0 ethyl 3-oxo-3-phenylpropionate 
• 120-46-7 1,3-diphenylpropanedione 
• 623-49-4 ethyl cyanoformate 
• 98-86-2 acetophenone 

Downstream Products

• 46460-23-5 ethyl L-2-amino-4-phenylbutyrate 
• 94815-37-9 2-buten-1-one-3-amino-4-hydroxy-1-phenyl 
• 94815-41-5 2-penten-1-one-3-amino-4-hydroxy-4-methyl-1-phenyl 

Relevant articles and documents

Formation of functionalized 2H-azirines through phio-mediated trifluoroethoxylation and azirination of enamines

A variety of enaminones and enamine carboxylic esters were converted to trifluoroethoxylated 2H-azirines through reactions with PhIO in trifluoroethanol (TFE). The cascade reaction is postulated to proceed via a PhIO-mediated oxidative trifluoroethoxylation and a subsequent azirination of the α-trifluoroethoxylated enamine intermediates.

Method for transferring amino acid into ketone acid(ester)

A method for transferring amino acid into ketone acid (ester) may obtain ketone acid (ester) at low cost. The method uses sodium hypochlorous acid as oxidizing agent and proceeds oxidation reaction with amino acid or its derivatives so as to obtain ketone acid and its derivatives. The sodium hypochlorous acid is easily to get with low cost and the conditions of the reaction are mild so that the method meets the needs of the industry.

Ethyl 2,4-dioxoalkanoates as starting materials for a convenient route to 3(2H)furanones and 3(2H)furanimines

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