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855259-86-8

Ac-Glu-Gly-Lys-Cys(Glcβ1)-Gly-SBn is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 855259-86-8 Structure

  • Basic information

    1. Product Name: Ac-Glu-Gly-Lys-Cys(Glcβ1)-Gly-SBn
    2. Synonyms: Ac-Glu-Gly-Lys-Cys(Glcβ1)-Gly-SBn
    3. CAS NO:855259-86-8
    4. Molecular Formula:
    5. Molecular Weight: 802.924
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 855259-86-8.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Ac-Glu-Gly-Lys-Cys(Glcβ1)-Gly-SBn(CAS DataBase Reference)
    10. NIST Chemistry Reference: Ac-Glu-Gly-Lys-Cys(Glcβ1)-Gly-SBn(855259-86-8)
    11. EPA Substance Registry System: Ac-Glu-Gly-Lys-Cys(Glcβ1)-Gly-SBn(855259-86-8)

  • 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: 855259-86-8(Hazardous Substances Data)

855259-86-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 855259-86-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,5,2,5 and 9 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 855259-86:
(8*8)+(7*5)+(6*5)+(5*2)+(4*5)+(3*9)+(2*8)+(1*6)=208
208 % 10 = 8
So 855259-86-8 is a valid CAS Registry Number.

855259-86-8Downstream Products

855259-86-8Relevant articles and documents

Aziridine-2-carboxylic acid-containing peptides: Application to solution- and solid-phase convergent site-selective peptide modification

Galonic, Danica P.,Ide, Nathan D.,Van Der Donk, Wilfred A.,Gin, David Y.

, p. 7359 - 7369 (2007/10/03)

The development of a method for site- and stereoselective peptide modification using aziridine-2-carboxylic acid-containing peptides is described. A solid-phase peptide synthesis methodology that allows for the rapid generation of peptides incorporating the aziridine residue has been developed. The unique electrophilic nature of this nonproteinogenic amino acid allows for site-selective conjugation with various thiol nucleophiles, such as anomeric carbohydrate thiols, farnesyl thiol, and biochemical tags, both in solution and on solid support. This strategy, combined with native chemical ligation, provides convergent and rapid access to complex thioglycoconjugates.

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