56598-30-2

Basic information

• Product Name: (S)-N-1-ethoxycarbonyl-2-phenylethylacrylamide
• Synonyms: (S)-N-1-ethoxycarbonyl-2-phenylethylacrylamide
• CAS NO: 56598-30-2
• Molecular Weight: 247.294
• Mol File: 56598-30-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (S)-N-1-ethoxycarbonyl-2-phenylethylacrylamide(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-N-1-ethoxycarbonyl-2-phenylethylacrylamide(56598-30-2)
• EPA Substance Registry System: (S)-N-1-ethoxycarbonyl-2-phenylethylacrylamide(56598-30-2)

Safety Data

• Hazardous Substances Data: 56598-30-2(Hazardous Substances Data)

Upstream product

• 3081-24-1 H-Phe-OEt 
• 814-68-6 acryloyl chloride 
• 3182-93-2 (L)-phenylalanine ethyl ester hydrochloride 
• 2051-76-5 acrylic acid anhydride 

Downstream Products

• 1338067-97-2 C₂₃H₂₅NO₄ 
• 1338067-84-7 C₁₈H₂₇NO₃Si 
• 904927-44-2 N,N'-bis[(S)-1-(ethoxycarbonyl)-2-phenylethyl]fumaric diamide 

Relevant articles and documents

A microwave enhanced cross-metathesis approach to peptidomimetics

Functionalization of amino acid C- and N-termini with appropriate olefinic moieties allows for the generation of a peptidomimetic via a stereoselective cross-metathesis. This journal is The Royal Society of Chemistry.

Synthesis of small tripeptide molecules through a catalysis sequence comprising metathesis and aminohydroxylation

Tripeptidic structures were synthesized by using a combination of two independent consecutive catalytic procedures. Cross-metathesis of N-acroyl amino acid esters yields fumaric amide compounds with exclusive E double-bond geometry. This represents an unp