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5,6-difluoro-2-(4-methylphenyl)-1,3-benzothiazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1312920-13-0 Structure
  • Basic information

    1. Product Name: 5,6-difluoro-2-(4-methylphenyl)-1,3-benzothiazole
    2. Synonyms: 5,6-difluoro-2-(4-methylphenyl)-1,3-benzothiazole
    3. CAS NO:1312920-13-0
    4. Molecular Formula:
    5. Molecular Weight: 261.295
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1312920-13-0.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: 5,6-difluoro-2-(4-methylphenyl)-1,3-benzothiazole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5,6-difluoro-2-(4-methylphenyl)-1,3-benzothiazole(1312920-13-0)
    11. EPA Substance Registry System: 5,6-difluoro-2-(4-methylphenyl)-1,3-benzothiazole(1312920-13-0)
  • 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: 1312920-13-0(Hazardous Substances Data)

1312920-13-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1312920-13-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,2,9,2 and 0 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1312920-13:
(9*1)+(8*3)+(7*1)+(6*2)+(5*9)+(4*2)+(3*0)+(2*1)+(1*3)=110
110 % 10 = 0
So 1312920-13-0 is a valid CAS Registry Number.

1312920-13-0Downstream Products

1312920-13-0Relevant articles and documents

Synthesis, anticancer activity and docking of some substituted benzothiazoles as tyrosine kinase inhibitors

Bhuva, Hemal A.,Kini, Suvarna G.

, p. 32 - 37 (2011/10/09)

Protein tyrosine kinases occupy a central position in the control of cellular proliferation and its inactivation might lead to the discovery of a new generation anticancer compounds. Substituted benzothiazoles have been found to mimic the ATP-competitive

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