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  • 1276039-85-0 Structure
  • Basic information

    1. Product Name: C21H14F6N2O3
    2. Synonyms: C21H14F6N2O3
    3. CAS NO:1276039-85-0
    4. Molecular Formula:
    5. Molecular Weight: 456.344
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1276039-85-0.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: C21H14F6N2O3(CAS DataBase Reference)
    10. NIST Chemistry Reference: C21H14F6N2O3(1276039-85-0)
    11. EPA Substance Registry System: C21H14F6N2O3(1276039-85-0)
  • 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: 1276039-85-0(Hazardous Substances Data)

1276039-85-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1276039-85-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,7,6,0,3 and 9 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1276039-85:
(9*1)+(8*2)+(7*7)+(6*6)+(5*0)+(4*3)+(3*9)+(2*8)+(1*5)=170
170 % 10 = 0
So 1276039-85-0 is a valid CAS Registry Number.

1276039-85-0Relevant articles and documents

Structure-based design of novel HCV NS5B thumb pocket 2 allosteric inhibitors with submicromolar gt1 replicon potency: Discovery of a quinazolinone chemotype

Beaulieu, Pierre L.,Coulombe, René,Duan, Jianmin,Fazal, Gulrez,Godbout, Cédrickx,Hucke, Oliver,Jakalian, Araz,Joly, Marc-André,Lepage, Olivier,Llinàs-Brunet, Montse,Naud, Julie,Poirier, Martin,Rioux, Nathalie,Thavonekham, Bounkham,Kukolj, George,Stammers, Timothy A.

, p. 4132 - 4140 (2013/07/25)

We describe the structure-based design of a novel lead chemotype that binds to thumb pocket 2 of HCV NS5B polymerase and inhibits cell-based gt1 subgenomic reporter replicons at sub-micromolar concentrations (EC50 200 nM). This new class of po

QUINAZOLINONE DERIVATIVES AS VIRAL POLYMERASE INHIBITORS

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Page/Page column 43, (2011/04/19)

Compounds of formula I: (I) wherein X, R2, R3, R5 and R6 are defined herein, are useful as inhibitors of the hepatitis C virus NS5B polymerase.

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