1005192-53-9

Basic information

• Product Name: (3R,6S)-1-benzyl-3-(2-dibenzylaminoethyl)-5-ethoxy-1,6-dihydro-6-isopropylpyrazin-2-(3H)-one
• Synonyms: (3R,6S)-1-benzyl-3-(2-dibenzylaminoethyl)-5-ethoxy-1,6-dihydro-6-isopropylpyrazin-2-(3H)-one
• CAS NO: 1005192-53-9
• Molecular Weight: 497.681
• Mol File: 1005192-53-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (3R,6S)-1-benzyl-3-(2-dibenzylaminoethyl)-5-ethoxy-1,6-dihydro-6-isopropylpyrazin-2-(3H)-one(CAS DataBase Reference)
• NIST Chemistry Reference: (3R,6S)-1-benzyl-3-(2-dibenzylaminoethyl)-5-ethoxy-1,6-dihydro-6-isopropylpyrazin-2-(3H)-one(1005192-53-9)
• EPA Substance Registry System: (3R,6S)-1-benzyl-3-(2-dibenzylaminoethyl)-5-ethoxy-1,6-dihydro-6-isopropylpyrazin-2-(3H)-one(1005192-53-9)

Safety Data

• Hazardous Substances Data: 1005192-53-9(Hazardous Substances Data)

Upstream product

• 109651-07-2 1-(N,N-dibenzylamino)-2-iodoethane 
• 433735-03-6 (6S)-1-benzyl-5-ethoxy-3,6-dihydro-6-isopropylpyrazine-2-one 

Downstream Products

• 1005192-58-4 (3R,6S)-1-benzyl-3-(2-aminoethyl)-5-ethoxy-1,6-dihydro-6-isopropylpyrazin-2-(3H)-one 
• 1268691-54-8 N₂-acetyl-N-{(1R)-3-(dibenzylamino)-1-{{[(1S)-1-(ethoxycarbonyl)-2-methylpropyl]amino}carbonyl}propyl}-2-methyl-D-asparaginyl-L-valine ethyl ester 
• 1268691-38-8 (3R,6S)-3-[2-(dibenzylamino)ethyl]-5-ethoxy-3,6-dihydro-6-isopropylpyrazin-2(1H)-one 
• 1268691-46-8 N-{(2R)-4-(dibenzylamino)-2-{{2-[(2R,5S)-6-ethoxy-2,3,4,5-tetrahydro-2-methyl-5-isopropyl-3-oxopyrazin-2-yl]acetyl}amino}-1-oxobutyl}-L-valine ethyl ester 

Relevant articles and documents

Stereoselective synthesis and conformational analysis of unnatural tetrapeptides. Part 2

Stereoselective synthesis of unnatural tetrapeptides 20a and 20b, 21a and 21b and 30 and 31, containing two l-valine units and two unnatural α-amino acids (ornithine and modified aspartic acid), has been accomplished starting from the l-valine derived chiral synthon 1. Structural investigations of these non-proteinogenic peptides have been carried out on the acetamido derivatives using 1H NMR, IR spectroscopic techniques and a conformational analysis based on molecular dynamics (MD) and cluster analysis.