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CAS

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1292821-09-0

C17H14ClN3O3S is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1292821-09-0 Structure

  • Basic information

    1. Product Name: C17H14ClN3O3S
    2. Synonyms: C17H14ClN3O3S
    3. CAS NO:1292821-09-0
    4. Molecular Formula:
    5. Molecular Weight: 375.835
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1292821-09-0.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: C17H14ClN3O3S(CAS DataBase Reference)
    10. NIST Chemistry Reference: C17H14ClN3O3S(1292821-09-0)
    11. EPA Substance Registry System: C17H14ClN3O3S(1292821-09-0)

  • 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: 1292821-09-0(Hazardous Substances Data)

1292821-09-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1292821-09-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,9,2,8,2 and 1 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1292821-09:
(9*1)+(8*2)+(7*9)+(6*2)+(5*8)+(4*2)+(3*1)+(2*0)+(1*9)=160
160 % 10 = 0
So 1292821-09-0 is a valid CAS Registry Number.

1292821-09-0Downstream Products

1292821-09-0Relevant articles and documents

2-(4-Carbonylphenyl)benzoxazole inhibitors of CETP: Scaffold design and advancement in HDLc-raising efficacy

Sweis, Ramzi F.,Hunt, Julianne A.,Kallashi, Florida,Hammond, Milton L.,Chen, Ying,Eveland, Suzanne S.,Guo, Qiu,Hyland, Sheryl A.,Milot, Denise P.,Cumiskey, Anne-Marie,Latham, Melanie,Rosa, Raymond,Peterson, Larry,Sparrow, Carl P.,Wright, Samuel D.,Anderson, Matt S.,Sinclair, Peter J.

, p. 1890 - 1895 (2011)

The development of 2-phenylbenzoxazoles as inhibitors of cholesteryl ester transfer protein (CETP) is described. Initial efforts aimed at engineering replacements for the aniline substructures in the benchmark molecule. Reversing the connectivity of the central aniline lead to a new class of 2-(4-carbonylphenyl)benzoxazoles. Structure-activity studies at the C-7 and terminal pyridine ring allowed for the optimization of potency and HDLc-raising efficacy in this new class of inhibitors. These efforts lead to the discovery of benzoxazole 11v, which raised HDLc by 24 mg/dl in our transgenic mouse PD model.

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