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cyclo(-D(tBu)-f-K(Aloc)-R(Pmc)-G-) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 343312-39-0 Structure
  • Basic information

    1. Product Name: cyclo(-D(tBu)-f-K(Aloc)-R(Pmc)-G-)
    2. Synonyms: cyclo(-D(tBu)-f-K(Aloc)-R(Pmc)-G-)
    3. CAS NO:343312-39-0
    4. Molecular Formula:
    5. Molecular Weight: 1010.22
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 343312-39-0.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: cyclo(-D(tBu)-f-K(Aloc)-R(Pmc)-G-)(CAS DataBase Reference)
    10. NIST Chemistry Reference: cyclo(-D(tBu)-f-K(Aloc)-R(Pmc)-G-)(343312-39-0)
    11. EPA Substance Registry System: cyclo(-D(tBu)-f-K(Aloc)-R(Pmc)-G-)(343312-39-0)
  • 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: 343312-39-0(Hazardous Substances Data)

343312-39-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 343312-39-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,3,3,1 and 2 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 343312-39:
(8*3)+(7*4)+(6*3)+(5*3)+(4*1)+(3*2)+(2*3)+(1*9)=110
110 % 10 = 0
So 343312-39-0 is a valid CAS Registry Number.

343312-39-0Relevant articles and documents

A convenient access to αVβ3/αVβ5 integrin ligand conjugates: Regioselective solid-phase functionalisation of an RGD based peptide

Boturyn, Didier,Dumy, Pascal

, p. 2787 - 2790 (2001)

The cyclopeptide (-RGDfK-) is a potent and selective αVβ3/αVβ5 integrin ligand. A methodology for the conjugation of cyclo(-RGDfK-) through the regioselective derivatisation of lysine side chains, either in solution or directly on the solid support, is described. This provides a rapid and flexible chemical entry to conjugated integrin ligands bearing reporter groups for biological investigations or reactive chemical functions for the preparation of new vector systems.

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