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C45H62N6O10*C2HF3O2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1453341-02-0 Structure
  • Basic information

    1. Product Name: C45H62N6O10*C2HF3O2
    2. Synonyms: C45H62N6O10*C2HF3O2
    3. CAS NO:1453341-02-0
    4. Molecular Formula:
    5. Molecular Weight: 961.045
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1453341-02-0.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: C45H62N6O10*C2HF3O2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C45H62N6O10*C2HF3O2(1453341-02-0)
    11. EPA Substance Registry System: C45H62N6O10*C2HF3O2(1453341-02-0)
  • 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: 1453341-02-0(Hazardous Substances Data)

1453341-02-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1453341-02-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,5,3,3,4 and 1 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1453341-02:
(9*1)+(8*4)+(7*5)+(6*3)+(5*3)+(4*4)+(3*1)+(2*0)+(1*2)=130
130 % 10 = 0
So 1453341-02-0 is a valid CAS Registry Number.

1453341-02-0Relevant articles and documents

Synthesis of cyclic peptide hemicryptophanes: Enantioselective recognition of a chiral zwitterionic guest

Cochrane, James R.,Schmitt, Aline,Wille, Uta,Hutton, Craig A.

, p. 8504 - 8506 (2013)

The synthesis of the first members of a new class of cyclic peptide-containing hemicryptophanes is described. Synthesis was achieved through attachment of veratryl groups to the l-tyrosine side chains of a cyclic hexapeptide, c(YG)3, followed by intramolecular cyclodehydration to generate the CTV unit. The diastereomeric P- and M-hemicryptophanes were generated in a 2 : 1 ratio and were separated by chromatography. The enantioselective binding properties of the hemicryptophanes were investigated by complexation with carnitine. Both isomers were found to have significant selectivity for binding (R)-carnitine. The Royal Society of Chemistry 2013.

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