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CAS

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1380167-27-0

C31H40N10O10S2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1380167-27-0 Structure

  • Basic information

    1. Product Name: C31H40N10O10S2
    2. Synonyms: C31H40N10O10S2
    3. CAS NO:1380167-27-0
    4. Molecular Formula:
    5. Molecular Weight: 776.852
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1380167-27-0.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: C31H40N10O10S2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C31H40N10O10S2(1380167-27-0)
    11. EPA Substance Registry System: C31H40N10O10S2(1380167-27-0)

  • 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: 1380167-27-0(Hazardous Substances Data)

1380167-27-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1380167-27-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,0,1,6 and 7 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1380167-27:
(9*1)+(8*3)+(7*8)+(6*0)+(5*1)+(4*6)+(3*7)+(2*2)+(1*7)=150
150 % 10 = 0
So 1380167-27-0 is a valid CAS Registry Number.

1380167-27-0Downstream Products

1380167-27-0Relevant articles and documents

Synthesis and binding properties of new selective ligands for the nucleobase opposite the AP site

Abe, Yukiko,Nakagawa, Osamu,Yamaguchi, Rie,Sasaki, Shigeki

, p. 3470 - 3479 (2012/08/08)

DNA is continuously damaged by endogenous and exogenous factors such as oxidative stress or DNA alkylating agents. These damaged nucleobases are removed by DNA N-glycosylase and form apurinic/apyrimidinic sites (AP sites) as intermediates in the base exci

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