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CAS

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863227-27-4

C26H23Cl2N5O4 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 863227-27-4 Structure

  • Basic information

    1. Product Name: C26H23Cl2N5O4
    2. Synonyms:
    3. CAS NO:863227-27-4
    4. Molecular Formula:
    5. Molecular Weight: 540.406
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 863227-27-4.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: C26H23Cl2N5O4(CAS DataBase Reference)
    10. NIST Chemistry Reference: C26H23Cl2N5O4(863227-27-4)
    11. EPA Substance Registry System: C26H23Cl2N5O4(863227-27-4)

  • 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: 863227-27-4(Hazardous Substances Data)

863227-27-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 863227-27-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,3,2,2 and 7 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 863227-27:
(8*8)+(7*6)+(6*3)+(5*2)+(4*2)+(3*7)+(2*2)+(1*7)=174
174 % 10 = 4
So 863227-27-4 is a valid CAS Registry Number.

863227-27-4Downstream Products

863227-27-4Relevant articles and documents

Synthesis and SAR of pyridazinone-substituted phenylalanine amide α4 integrin antagonists

Gong, Yong,Kent Barbay,Kimball, Edward S.,Santulli, Rosemary J.,Carolyn Fisher,Dyatkin, Alexey B.,Miskowski, Tamara A.,Hornby, Pamela J.,He, Wei

, p. 1331 - 1335 (2008)

Structural modification and cellular adhesion inhibition activities of pyridazinone-substituted phenylalanine amide α4 integrin antagonists are described. Functionality requirements for the arylamide moiety and the carboxylic acid group were de

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