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1019975-15-5

C16H17NO3*ClH is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1019975-15-5 Structure

  • Basic information

    1. Product Name: C16H17NO3*ClH
    2. Synonyms:
    3. CAS NO:1019975-15-5
    4. Molecular Formula:
    5. Molecular Weight: 307.777
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1019975-15-5.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: C16H17NO3*ClH(CAS DataBase Reference)
    10. NIST Chemistry Reference: C16H17NO3*ClH(1019975-15-5)
    11. EPA Substance Registry System: C16H17NO3*ClH(1019975-15-5)

  • 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: 1019975-15-5(Hazardous Substances Data)

1019975-15-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1019975-15-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,1,9,9,7 and 5 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1019975-15:
(9*1)+(8*0)+(7*1)+(6*9)+(5*9)+(4*7)+(3*5)+(2*1)+(1*5)=165
165 % 10 = 5
So 1019975-15-5 is a valid CAS Registry Number.

1019975-15-5Relevant articles and documents

Synthesis and biological evaluation of imidazol-2-one derivatives as potential antitumor agents

Xue, Na,Yang, Xiaochun,Wu, Rui,Chen, Jing,He, Qiaojun,Yang, Bo,Lu, Xiuyang,Hu, Yongzhou

, p. 2550 - 2557 (2008)

A new series of aryl substituted imidazol-2-one derivatives structurally related to combretastatin A-4 (CA-4) were synthesized and evaluated for their cytotoxic activities in vitro against various human cancer cell lines including MDR cell line. The cytotoxic effects of compounds 7b and 7i proved to be similar to or greater than that of docetaxel. The highly active compound 7b also exhibited excellent inhibitory activity on tumor growth in vivo.

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