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CAS

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85003-76-5

BOC-CYS(Z-AMINOETHYL)-OH, also known as Boc-S-Z-aminoethyl-L-cysteine, is a chemical compound that serves as a valuable intermediate in the synthesis of various biologically active molecules. It is characterized by the presence of a protected cysteine residue with a Z-aminoethyl group, which plays a crucial role in the formation of peptide bonds and the development of peptide-based therapeutics.

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  • 85003-76-5 Structure

  • Basic information

    1. Product Name: BOC-CYS(Z-AMINOETHYL)-OH
    2. 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
    3. CAS NO:85003-76-5
    4. Molecular Formula: C18H26N2O6S
    5. Molecular Weight: 398.47
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 85003-76-5.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: -15°C
    8. Solubility: N/A
    9. CAS DataBase Reference: BOC-CYS(Z-AMINOETHYL)-OH(CAS DataBase Reference)
    10. NIST Chemistry Reference: BOC-CYS(Z-AMINOETHYL)-OH(85003-76-5)
    11. EPA Substance Registry System: BOC-CYS(Z-AMINOETHYL)-OH(85003-76-5)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 85003-76-5(Hazardous Substances Data)

85003-76-5 Usage

Uses

Used in Pharmaceutical Industry:
BOC-CYS(Z-AMINOETHYL)-OH is used as a key intermediate in the synthesis of Somatostatin (S676753) analogs for the treatment of various medical conditions. Its unique structure allows for the development of peptide-based drugs with improved stability, bioavailability, and therapeutic efficacy.

Check Digit Verification of cas no

The CAS Registry Mumber 85003-76-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,0,0 and 3 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 85003-76:
(7*8)+(6*5)+(5*0)+(4*0)+(3*3)+(2*7)+(1*6)=115
115 % 10 = 5
So 85003-76-5 is a valid CAS Registry Number.

85003-76-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 10-Oxa-5-thia-2,8-diazadodecanoicacid, 7-carboxy-11,11-dimethyl-9-oxo-, 1-(phenylmethyl) ester, (7R)-

1.2 Other means of identification

Product number -
Other names (R)-3-(2-benzyloxycarbonylaminoethylsulfanyl)-2-tert-butoxycarbonylaminopropionic acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:85003-76-5 SDS

85003-76-5Relevant articles and documents

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

Young, Robert J.,Beams, Richard M.,Carter, Keith,Clark, Helen A.R.,Coe, Diane M.,Chambers, C. Lynn,Davies, P. Ifeyinwa,Dawson, John,Drysdale, Martin J.,Franzman, Karl W.,French, Colin,Hodgson, Simon T.,Hodson, Harold F.,Kleanthous, Savvas,Rider, Peter,Sanders, Daniela,Sawyer, David A.,Scott, Keith J.,Shearer, Barry G.,Stocker, Richard,Smith, Steven,Tackley, Miriam C.,Knowles, Richard G.

, p. 597 - 600 (2007/10/03)

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.

PERHYDRO-1,4-THIAZEPIN-5-ONE AND PERHYDRO-1,4-THIAZOCIN-5-ONE DERIVATIVES AS ANTIHYPERTENSIVES

-

, (2008/06/13)

There are disclosed perhydro-1,4-thiazepin-5-one and perhydro-1,4-thiazocin-5-one derivatives and related compounds which are useful as angiotensin converting enzyme inhibitors and as antihypertensives.

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