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1042360-64-4

C26H20ClN3O3S3 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1042360-64-4 Structure

  • Basic information

    1. Product Name: C26H20ClN3O3S3
    2. Synonyms:
    3. CAS NO:1042360-64-4
    4. Molecular Formula:
    5. Molecular Weight: 554.114
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1042360-64-4.mol
    9. Article Data: 1

  • 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: C26H20ClN3O3S3(CAS DataBase Reference)
    10. NIST Chemistry Reference: C26H20ClN3O3S3(1042360-64-4)
    11. EPA Substance Registry System: C26H20ClN3O3S3(1042360-64-4)

  • 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: 1042360-64-4(Hazardous Substances Data)

1042360-64-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1042360-64-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,4,2,3,6 and 0 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1042360-64:
(9*1)+(8*0)+(7*4)+(6*2)+(5*3)+(4*6)+(3*0)+(2*6)+(1*4)=104
104 % 10 = 4
So 1042360-64-4 is a valid CAS Registry Number.

1042360-64-4Downstream Products

1042360-64-4Relevant articles and documents

Synthesis, anti-HIV-1 integrase, and cytotoxic activities of 4-chloro-N-(4-oxopyrimidin-2-yl)-2-mercaptobenzenesulfonamide derivatives

Brzozowski, Zdzislaw,Slawinski, Jaroslaw,Saczewski, Franciszek,Sanchez, Tino,Neamati, Nouri

, p. 1188 - 1198 (2008/09/20)

Several 4-chloro-N-(4-oxopyrimidin-2-yl)-2-mercaptobenzenesulfonamide derivatives 13-28 and 35-44 have been synthesized and tested as potential HIV-1 integrase (IN) inhibitors. Compounds 15-17, 19, 21-28, 36 and 41 inhibited IN with IC50 values in the range of 3.3-63.0 μM. The compounds 13, 15, 16, 21-24 and 26-28 were further tested at the US National Cancer Institute for their in vitro activity against a panel of 53-57 human tumor cell lines. The compounds 26-28 were inactive, whereas the other compounds exhibited high or reasonable activity (GI50 0.01-20.0 μM) against one or more human tumor cell lines.

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