85003-76-5

Basic information

• Product Name: BOC-CYS(Z-AMINOETHYL)-OH
• Synonyms: N-ALPHA-T-BUTOXYCARBONYL, N-EPSILON-CARBOBENZOXY-S-2-AMINOETHYL-L-CYSTEINE;BOC-S-Z-AMINOETHYL-L-CYSTEINE;BOC-CYSTEINE(Z-AMINOETHYL)-OH;BOC-CYS(Z-AMINOETHYL)-OH;BOC-CYS(Z-NHET)-OH;BOC-CYS(ET-NH-Z)-OH;Boc-L-4-thialysine(Z)-OH;Boc-L-Cys(Z-NHEt)-OH
• CAS NO: 85003-76-5
• Molecular Formula: C₁₈H₂₆N₂O₆S
• Molecular Weight: 398.47
• Mol File: 85003-76-5.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• Storage Temp.: -15°C
• CAS DataBase Reference: BOC-CYS(Z-AMINOETHYL)-OH(CAS DataBase Reference)
• NIST Chemistry Reference: BOC-CYS(Z-AMINOETHYL)-OH(85003-76-5)
• EPA Substance Registry System: BOC-CYS(Z-AMINOETHYL)-OH(85003-76-5)

Safety Data

• Hazardous Substances Data: 85003-76-5(Hazardous Substances Data)

Usage

Chemical Properties

Clear, colorless oil

Uses

Boc-S-Z-aminoethyl-L-cysteine is a useful intermediate, used in the preparation of Somatostatin (S676753) analogs.

Upstream product

• 24424-99-5 di-tert-butyl dicarbonate 
• 41889-04-7 S-(2-benzyloxycarbonylamino-ethyl)-L-cysteine 

Downstream Products

• 1198185-70-4 benzyl (R)-3-(2-benzyloxycarbonylaminoethanesulfonyl)-2-[3-((9S,12R)-9-isopropyl-11-oxo-2,7-dioxa-10-azabicyclo[12.2.2]octadeca-1⁽¹⁷⁾,14⁽¹⁸⁾,15-trien-12-yl)ureido]propionate 
• 1198185-68-0 Benzyl (R)-3-(2-benzyloxycarbonylaminoethylsulfanyl)-2-[3-((9S,12R)-9-isopropyl-11-oxo-2,7-dioxa-10-azabicyclo[12.2.2]octadeca-1⁽¹⁷⁾,14⁽¹⁸⁾,15-trien-12-yl)ureido]propionate 
• 732211-08-4 Benzyl (R)-2-amino-3-(2-benzyloxycarbonylaminoethylsulfanyl)propionate 
• 1198185-64-6 Benzyl (R)-3-(2-benzyloxycarbonylaminoethylsulfanyl)-2-tert-butoxycarbonylaminopropionate 

Relevant articles and documents

Inhibition of inducible nitric oxide synthase by acetamidine derivatives of hetero-substituted lysine and homolysine

The synthesis and in vitro evaluation of the acetamidine derivatives of hetero-substituted lysine and homolysine analogues have identified potent inhibitors of human nitric oxide synthase enzymes, including examples with marked selectivity for the inducible isoform. (C) 2000 Elsevier Science Ltd. All rights reserved.