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1600519-28-5

C17H17NO4S is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1600519-28-5 Structure

  • Basic information

    1. Product Name: C17H17NO4S
    2. Synonyms: C17H17NO4S
    3. CAS NO:1600519-28-5
    4. Molecular Formula:
    5. Molecular Weight: 331.392
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1600519-28-5.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: C17H17NO4S(CAS DataBase Reference)
    10. NIST Chemistry Reference: C17H17NO4S(1600519-28-5)
    11. EPA Substance Registry System: C17H17NO4S(1600519-28-5)

  • 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: 1600519-28-5(Hazardous Substances Data)

1600519-28-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1600519-28-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,0,0,5,1 and 9 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1600519-28:
(9*1)+(8*6)+(7*0)+(6*0)+(5*5)+(4*1)+(3*9)+(2*2)+(1*8)=125
125 % 10 = 5
So 1600519-28-5 is a valid CAS Registry Number.

1600519-28-5Relevant articles and documents

Synthesis and structure activity relationships of schweinfurthin indoles

Kodet, John G.,Beutler, John A.,Wiemer, David F.

, p. 2542 - 2552 (2014)

As part of a program to explore the biological activity of analogues of the natural schweinfurthins, a set of compounds has been prepared where an indole system can be viewed as a substitution for the resorcinol substructure of the schweinfurthin's D-ring. Twelve of these schweinfurthin indoles have been prepared and evaluated in the 60 cell line screen of the National Cancer Institute. While a range of activity has been observed, it is now clear that schweinfurthin indoles can demonstrate the intriguing pattern of activity associated with the natural stilbenes. In the best cases, these indole analogues display both potency and differential activity across the various cell lines comparable to the best resorcinol analogues.

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