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859838-12-3

C21H24FN5O3S is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 859838-12-3 Structure

  • Basic information

    1. Product Name: C21H24FN5O3S
    2. Synonyms:
    3. CAS NO:859838-12-3
    4. Molecular Formula:
    5. Molecular Weight: 445.518
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 859838-12-3.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: C21H24FN5O3S(CAS DataBase Reference)
    10. NIST Chemistry Reference: C21H24FN5O3S(859838-12-3)
    11. EPA Substance Registry System: C21H24FN5O3S(859838-12-3)

  • 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: 859838-12-3(Hazardous Substances Data)

859838-12-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 859838-12-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,9,8,3 and 8 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 859838-12:
(8*8)+(7*5)+(6*9)+(5*8)+(4*3)+(3*8)+(2*1)+(1*2)=233
233 % 10 = 3
So 859838-12-3 is a valid CAS Registry Number.

859838-12-3Downstream Products

859838-12-3Relevant articles and documents

3,4-Diamino-2,5-thiadiazole-1-oxides as potent CXCR2/CXCR1 antagonists

Biju, Purakkattle,Taveras, Arthur,Yu, Younong,Zheng, Junying,Chao, Jianhua,Rindgen, Diane,Jakway, James,Hipkin, R. William,Fossetta, James,Fan, Xuedong,Fine, Jay,Qiu, Hongchen,Merritt, J. Robert,Baldwin, John J.

, p. 228 - 231 (2008/09/17)

A series of novel and potent 3,4-diamino-2,5-thiadiazole-1-oxides were prepared and found to show excellent binding affinities for CXCR2 and CXCR1 receptors and excellent inhibitory activity of Gro-α and IL-8 mediated in vitro hPMN MPO release of CXCR2 an

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