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1011469-69-4

C28H28FN3O5 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1011469-69-4 Structure

  • Basic information

    1. Product Name: C28H28FN3O5
    2. Synonyms:
    3. CAS NO:1011469-69-4
    4. Molecular Formula:
    5. Molecular Weight: 505.546
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1011469-69-4.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: C28H28FN3O5(CAS DataBase Reference)
    10. NIST Chemistry Reference: C28H28FN3O5(1011469-69-4)
    11. EPA Substance Registry System: C28H28FN3O5(1011469-69-4)

  • 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: 1011469-69-4(Hazardous Substances Data)

1011469-69-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1011469-69-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,1,1,4,6 and 9 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1011469-69:
(9*1)+(8*0)+(7*1)+(6*1)+(5*4)+(4*6)+(3*9)+(2*6)+(1*9)=114
114 % 10 = 4
So 1011469-69-4 is a valid CAS Registry Number.

1011469-69-4Downstream Products

1011469-69-4Relevant articles and documents

Synthesis and structure-activity relationship studies of tyrosine-based antagonists at the human P2X7 receptor

Lee, Ga Eun,Joshi, Bhalchandra V.,Chen, Wangzhong,Jeong, Lak Shin,Moon, Hyung Ryong,Jacobson, Kenneth A.,Kim, Yong-Chul

, p. 571 - 575 (2008/09/20)

Analogues of the P2X7 receptor antagonist KN-62, modified at the piperazine and arylsulfonyl groups, were synthesized and assayed at the human P2X7 receptor for inhibition of BzATP-induced effects, that is, uptake of a fluorescent dy

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