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135924-21-9

Z-Phe-Gly(Br)-OMe is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 135924-21-9 Structure

  • Basic information

    1. Product Name: Z-Phe-Gly(Br)-OMe
    2. Synonyms:
    3. CAS NO:135924-21-9
    4. Molecular Formula:
    5. Molecular Weight: 449.301
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 135924-21-9.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: Z-Phe-Gly(Br)-OMe(CAS DataBase Reference)
    10. NIST Chemistry Reference: Z-Phe-Gly(Br)-OMe(135924-21-9)
    11. EPA Substance Registry System: Z-Phe-Gly(Br)-OMe(135924-21-9)

  • 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: 135924-21-9(Hazardous Substances Data)

135924-21-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 135924-21-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,9,2 and 4 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 135924-21:
(8*1)+(7*3)+(6*5)+(5*9)+(4*2)+(3*4)+(2*2)+(1*1)=129
129 % 10 = 9
So 135924-21-9 is a valid CAS Registry Number.

135924-21-9Downstream Products

135924-21-9Relevant articles and documents

CONVERSION OF SERINE AND THREONINE RESIDUES INTO α-ACYLOXY-, α-ALKYLTHIO-, AND α-HALOGENOGLYCINE MOIETIES: A NEW STRATEGY FOR THE MODIFICATION OF PEPTIDES

Apitz, Gregor,Steglich, Wolfgang

, p. 3163 - 3166 (2007/10/02)

Selective modification of serine and threonine containing peptides is accomplished by oxidation with lead tetraacetate.Conversion of the derived α-acetoxyglycine derivative into α-alkylthio- and α-halogenoglycine residues offers a novel synthetic route to

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