112157-36-5

Basic information

• Product Name: (S)-2-Amino-N-{(S)-1-[(S)-2-((S)-2-amino-3-phenyl-propionylamino)-4-methyl-pentyldisulfanylmethyl]-3-methyl-butyl}-3-phenyl-propionamide; compound with trifluoro-acetic acid
• CAS NO: 112157-36-5
• Molecular Weight: 786.901
• Mol File: 112157-36-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (S)-2-Amino-N-{(S)-1-[(S)-2-((S)-2-amino-3-phenyl-propionylamino)-4-methyl-pentyldisulfanylmethyl]-3-methyl-butyl}-3-phenyl-propionamide; compound with trifluoro-acetic acid(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-2-Amino-N-{(S)-1-[(S)-2-((S)-2-amino-3-phenyl-propionylamino)-4-methyl-pentyldisulfanylmethyl]-3-methyl-butyl}-3-phenyl-propionamide; compound with trifluoro-acetic acid(112157-36-5)
• EPA Substance Registry System: (S)-2-Amino-N-{(S)-1-[(S)-2-((S)-2-amino-3-phenyl-propionylamino)-4-methyl-pentyldisulfanylmethyl]-3-methyl-butyl}-3-phenyl-propionamide; compound with trifluoro-acetic acid(112157-36-5)

Safety Data

• Hazardous Substances Data: 112157-36-5(Hazardous Substances Data)

Upstream product

• 112157-33-2 (H-Leu(CH₂S)-)2*2HCl 
• 112157-32-1 [(S)-1-((S)-2-tert-Butoxycarbonylamino-4-methyl-pentyldisulfanylmethyl)-3-methyl-butyl]-carbamic acid tert-butyl ester 
• 112157-31-0 thioacetic acid S-((S)-2-tert-butoxycarbonylamino-4-methyl-pentyl) ester 
• 112157-30-9 (2S)-2-<(tert-butyloxycarbonyl)amino>-1-<(p-tolylsulfonyl)oxy>-4-methylpentane 
• 112157-38-7 tert-butyl (S)-(1-mercapto-4-methylpentan-2-yl)carbamate 
• 82010-31-9 (S)-(1-hydroxymethyl-3-methylbutyl)carbamic acid tert-butyl ester 
• 13734-34-4 N-tert-butoxycarbonyl-L-phenylalanine 
• 112157-34-3 ((S)-1-{(S)-1-[(S)-2-((S)-2-tert-Butoxycarbonylamino-3-phenyl-propionylamino)-4-methyl-pentyldisulfanylmethyl]-3-methyl-butylcarbamoyl}-2-phenyl-ethyl)-carbamic acid tert-butyl ester 
• 76-05-1 trifluoroacetic acid 

Downstream Products

• 112157-37-6 C₆₈H₉₆N₁₀O₁₄S₂ 

Relevant articles and documents

Synthesis of Enkephalin Analog with Leucinthiol at C-terminus as Probe for Thiol Group In Opiate Receptors

Enkephalin analog with thiol group at C-terminus, 2,Leu(CH2SH)5>enkephalin, was synthesized as possible probe for the essential thiol group in opiate receptors.In order to protect the free SH group of leucinthiol, oxidized Boc-