55636-11-8

Basic information

• Product Name: N-benzyl-2-(acetamido)-3-phenylacrylamide
• Synonyms: N-benzyl-2-(acetamido)-3-phenylacrylamide
• CAS NO: 55636-11-8
• Molecular Weight: 294.353
• Mol File: 55636-11-8.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: N-benzyl-2-(acetamido)-3-phenylacrylamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-benzyl-2-(acetamido)-3-phenylacrylamide(55636-11-8)
• EPA Substance Registry System: N-benzyl-2-(acetamido)-3-phenylacrylamide(55636-11-8)

Safety Data

• Hazardous Substances Data: 55636-11-8(Hazardous Substances Data)

Upstream product

• 100-46-9 benzylamine 
• 38879-46-8 (Z)-4-benzylidene-2-methyl-5(4H)-oxazolone 
• 100-52-7 benzaldehyde 
• 881-90-3 4-benzylidene-2-methyl-2-oxazolin-5-one 
• 88336-74-7 2-methyl-1,4-bis(phenylmethyl)-1H-imidazole 
• 143417-47-4 (4E)-2-methyl-4-(phenylmethylidene)-4,5-dihydro-1,3-oxazol-5-one 
• 55065-02-6 2-(N-acetylamino)cinnamic acid 
• 72015-61-3 (Z)-2-benzyloxycarbonylaminocinnamic acid 
• 74805-42-8 N-carboxy-α-dehydrophenylalanine anhydride 
• 80465-38-9 Ac-N-carboxy α-dehydrophenylalanine anhydride 

Downstream Products

• 156570-46-6 4-benzylidene-1-benzyl-2-methylimidazol-5-one 

Relevant articles and documents

Facile synthesis of 4-arylidene-5-imidazolinones as synthetic analogs of fluorescent protein chromophore

A facile and effective synthesis for a wide variety of 4-arylidene-5- imidazolinone derivatives was developed. 4-Arylidene-5-oxazolinones were prepared by Erlenmeyer azlactone synthesis from N-acylglycines and arylaldehydes. The ring-opening reactions of the 4-arylidene-5-oxazolinones with primary amines afforded 2-acylamino-3-arylacrylamides in excellent yields. A new dehydrative cyclization of the 2-acylamino-3-arylacrylamides in pyridine under reflux furnished the corresponding 4-arylidene-5-imidazolinones in good yields.

Heterocycles in Synthesis: Chiral Amino Acids/Dipeptides via a Novel Photooxidative Cleavage of Trisubstituted Imidazoles

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