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1016987-49-7

C20H35NO6SSi is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1016987-49-7 Structure

  • Basic information

    1. Product Name: C20H35NO6SSi
    2. Synonyms: C20H35NO6SSi
    3. CAS NO:1016987-49-7
    4. Molecular Formula:
    5. Molecular Weight: 445.653
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1016987-49-7.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: C20H35NO6SSi(CAS DataBase Reference)
    10. NIST Chemistry Reference: C20H35NO6SSi(1016987-49-7)
    11. EPA Substance Registry System: C20H35NO6SSi(1016987-49-7)

  • 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: 1016987-49-7(Hazardous Substances Data)

1016987-49-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1016987-49-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,1,6,9,8 and 7 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1016987-49:
(9*1)+(8*0)+(7*1)+(6*6)+(5*9)+(4*8)+(3*7)+(2*4)+(1*9)=167
167 % 10 = 7
So 1016987-49-7 is a valid CAS Registry Number.

1016987-49-7Downstream Products

1016987-49-7Relevant articles and documents

β-N-Biaryl ether sulfonamide hydroxamates as potent gelatinase inhibitors: Part 1. Design, synthesis, and lead identification

Yang, Shyh-Ming,Scannevin, Robert H.,Wang, Bingbing,Burke, Sharon L.,Wilson, Lawrence J.,Karnachi, Prabha,Rhodes, Kenneth J.,Lagu, Bharat,Murray, William V.

, p. 1135 - 1139 (2008/12/22)

A new series of β-N-biaryl ether sulfonamide hydroxamates as novel gelatinase inhibitors is described. These compounds exhibit good potency for MMP-2 and MMP-9 without inhibiting MMP-1. The structure-activity relationships (SAR) reveal the biaryl ether ty

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