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817624-22-9

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

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  • 817624-22-9 Structure

  • Basic information

    1. Product Name: Boc-Phe-Gly(OAc)-OMe
    2. Synonyms: Boc-Phe-Gly(OAc)-OMe
    3. CAS NO:817624-22-9
    4. Molecular Formula:
    5. Molecular Weight: 394.425
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 817624-22-9.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: Boc-Phe-Gly(OAc)-OMe(CAS DataBase Reference)
    10. NIST Chemistry Reference: Boc-Phe-Gly(OAc)-OMe(817624-22-9)
    11. EPA Substance Registry System: Boc-Phe-Gly(OAc)-OMe(817624-22-9)

  • 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: 817624-22-9(Hazardous Substances Data)

817624-22-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 817624-22-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,1,7,6,2 and 4 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 817624-22:
(8*8)+(7*1)+(6*7)+(5*6)+(4*2)+(3*4)+(2*2)+(1*2)=169
169 % 10 = 9
So 817624-22-9 is a valid CAS Registry Number.

817624-22-9Relevant articles and documents

An improved protocol for the SmI2-promoted C-alkylation of peptides: Degradation and functionalization of serine residues in linear and cyclic peptides

Blakskj?r, Peter,Gavrila, Adina,Andersen, Lisbeth,Skrydstrup, Troels

, p. 9091 - 9094 (2007/10/03)

The utility of the samarium diiodide promoted C-alkylation of peptides for the introduction of new side chains on peptide strands is dramatically enhanced by the initial oxidative degradation of serine residues in small peptides. In this way, cyclic pepti

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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