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1403815-62-2

C30H23BrN2O3 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1403815-62-2 Structure

  • Basic information

    1. Product Name: C30H23BrN2O3
    2. Synonyms:
    3. CAS NO:1403815-62-2
    4. Molecular Formula:
    5. Molecular Weight: 539.428
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1403815-62-2.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: C30H23BrN2O3(CAS DataBase Reference)
    10. NIST Chemistry Reference: C30H23BrN2O3(1403815-62-2)
    11. EPA Substance Registry System: C30H23BrN2O3(1403815-62-2)

  • 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: 1403815-62-2(Hazardous Substances Data)

1403815-62-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1403815-62-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,3,8,1 and 5 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1403815-62:
(9*1)+(8*4)+(7*0)+(6*3)+(5*8)+(4*1)+(3*5)+(2*6)+(1*2)=132
132 % 10 = 2
So 1403815-62-2 is a valid CAS Registry Number.

1403815-62-2Downstream Products

1403815-62-2Relevant articles and documents

Anti HIV-1 agents 6. Synthesis and anti-HIV-1 activity of indolyl glyoxamides

Wang, Yi,Huang, Ning,Yu, Xiang,Yang, Liu-Meng,Zhi, Xiao-Yan,Zheng, Yong-Tang,Xu, Hui

, p. 831 - 833 (2012/10/29)

In order to discover compounds with superior anti-human immunodeficiency virus type 1 (HIV-1) activity, 9 new indolyl glyoxamide derivatives (3a-i) were synthesized and preliminarily evaluated as HIV-1 inhibitors in vitro. Among all the derivatives, espec

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