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CAS

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1207477-04-0

C32H24FN3O3 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1207477-04-0 Structure

  • Basic information

    1. Product Name: C32H24FN3O3
    2. Synonyms:
    3. CAS NO:1207477-04-0
    4. Molecular Formula:
    5. Molecular Weight: 517.559
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1207477-04-0.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: C32H24FN3O3(CAS DataBase Reference)
    10. NIST Chemistry Reference: C32H24FN3O3(1207477-04-0)
    11. EPA Substance Registry System: C32H24FN3O3(1207477-04-0)

  • 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: 1207477-04-0(Hazardous Substances Data)

1207477-04-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1207477-04-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,7,4,7 and 7 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1207477-04:
(9*1)+(8*2)+(7*0)+(6*7)+(5*4)+(4*7)+(3*7)+(2*0)+(1*4)=140
140 % 10 = 0
So 1207477-04-0 is a valid CAS Registry Number.

1207477-04-0Downstream Products

1207477-04-0Relevant articles and documents

Pyrrole derivatives as potent inhibitors of lymphocyte-specific kinase: Structure, synthesis, and SAR

Takayama, Tetsuo,Umemiya, Hiroki,Amada, Hideaki,Yabuuchi, Tetsuya,Shiozawa, Fumiyasu,Katakai, Hironori,Takaoka, Akiko,Yamaguchi, Akie,Endo, Mayumi,Sato, Masakazu

, p. 108 - 111 (2010)

We have described the synthesis, enzyme inhibitory activity, structure-activity relationships, and proposed binding mode of a novel series of pyrrole derivatives as lymphocyte-specific kinase (Lck) inhibitors. The most potent analogs exhibited good enzyme inhibitory activity (IC50s 10 nM) for Lck kinase inhibition.

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