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913382-73-7

C14H12FNOS is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 913382-73-7 Structure

  • Basic information

    1. Product Name: C14H12FNOS
    2. Synonyms: C14H12FNOS
    3. CAS NO:913382-73-7
    4. Molecular Formula:
    5. Molecular Weight: 261.32
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 913382-73-7.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: C14H12FNOS(CAS DataBase Reference)
    10. NIST Chemistry Reference: C14H12FNOS(913382-73-7)
    11. EPA Substance Registry System: C14H12FNOS(913382-73-7)

  • 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: 913382-73-7(Hazardous Substances Data)

913382-73-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 913382-73-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,3,3,8 and 2 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 913382-73:
(8*9)+(7*1)+(6*3)+(5*3)+(4*8)+(3*2)+(2*7)+(1*3)=167
167 % 10 = 7
So 913382-73-7 is a valid CAS Registry Number.

913382-73-7Relevant 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

Antitumour properties of fluorinated benzothiazole-substituted hydroxycyclohexa-2,5-dienones ('quinols')

Lion, Cedric J.,Matthews, Charles S.,Wells, Geoffrey,Bradshaw, Tracey D.,Stevens, Malcolm F.G.,Westwell, Andrew D.

, p. 5005 - 5008 (2008/12/23)

The synthesis and in vitro antitumour evaluation of a new series of fluorinated benzothiazole-substituted 4-hydroxycyclohexa-2,5-dienones ('quinols') is described. The new compounds were found to be of comparable activity compared to the non-fluorinated precursor PMX 464, in terms of antiproliferative activity in sensitive human cancer cell lines (nanomolar GI50 values) and inhibitory activity against the thioredoxin signalling system.

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