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CAS

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948575-64-2

C12H9BrN4SO is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 948575-64-2 Structure

  • Basic information

    1. Product Name: C12H9BrN4SO
    2. Synonyms:
    3. CAS NO:948575-64-2
    4. Molecular Formula:
    5. Molecular Weight: 337.2
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 948575-64-2.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: C12H9BrN4SO(CAS DataBase Reference)
    10. NIST Chemistry Reference: C12H9BrN4SO(948575-64-2)
    11. EPA Substance Registry System: C12H9BrN4SO(948575-64-2)

  • 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: 948575-64-2(Hazardous Substances Data)

948575-64-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 948575-64-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,8,5,7 and 5 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 948575-64:
(8*9)+(7*4)+(6*8)+(5*5)+(4*7)+(3*5)+(2*6)+(1*4)=232
232 % 10 = 2
So 948575-64-2 is a valid CAS Registry Number.

948575-64-2Relevant articles and documents

Structure-based design, synthesis, and study of pyrazolo[1,5-a][1,3,5]triazine derivatives as potent inhibitors of protein kinase CK2

Nie, Zhe,Perretta, Carin,Erickson, Philip,Margosiak, Stephen,Almassy, Robert,Lu, Jia,Averill, April,Yager, Kraig M.,Chu, Shaosong

, p. 4191 - 4195 (2008/02/08)

The structure-based design, synthesis, and anticancer activity of novel inhibitors of protein kinase CK2 are described. Using pyrazolo[1,5-a][1,3,5]triazine as the core scaffold, a structure-guided series of modifications provided pM inhibitors with μM-le

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