1361510-35-1

Basic information

• Product Name: (S)-benzyl 1-(4-nitrophenylamino)-3-phenyl-1-selenoxopropan-2-ylcarbamate
• Synonyms: (S)-benzyl 1-(4-nitrophenylamino)-3-phenyl-1-selenoxopropan-2-ylcarbamate
• CAS NO: 1361510-35-1
• Molecular Weight: 482.397
• Mol File: 1361510-35-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (S)-benzyl 1-(4-nitrophenylamino)-3-phenyl-1-selenoxopropan-2-ylcarbamate(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-benzyl 1-(4-nitrophenylamino)-3-phenyl-1-selenoxopropan-2-ylcarbamate(1361510-35-1)
• EPA Substance Registry System: (S)-benzyl 1-(4-nitrophenylamino)-3-phenyl-1-selenoxopropan-2-ylcarbamate(1361510-35-1)

Safety Data

• Hazardous Substances Data: 1361510-35-1(Hazardous Substances Data)

Upstream product

• 14235-15-5 benzyl (S)-(1-((4-nitrophenyl)amino)-1-oxo-3-phenylpropan-2-yl)carbamate 
• 1161-13-3 N-Cbz-L-Phe 
• 100-01-6 4-nitro-aniline 

Relevant articles and documents

Synthesis of selenoxo peptides and oligoselenoxo peptides employing LiAlHSeH

Synthesis of selenoxo peptides by the treatment of Nα- protected peptide esters with a combination of PCl5 and LiAlHSeH is delineated. The method is simple, high-yielding, and free from racemization. Thus obtained selenoxo peptides are used as units for N-terminal chain extension through Nα-deprotection/coupling to yield peptide-selenoxo peptide hybrids. Multiple selenation is demonstrated by conversion of two peptide bonds of tripeptides into selenoxo peptide bonds. Amino acid derived arylamides are also converted into aryl selenoamides. C6H 5-CSeNH-Val-OMe 8f is obtained as single crystal, and its structure was determined through X-ray diffraction study.