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24615-03-0

1-<β-Oxo-propyloxy>-4--2-methyl-naphthalin is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 24615-03-0 Structure

  • Basic information

    1. Product Name: 1-<β-Oxo-propyloxy>-4--2-methyl-naphthalin
    2. Synonyms:
    3. CAS NO:24615-03-0
    4. Molecular Formula:
    5. Molecular Weight: 314.381
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 24615-03-0.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: 1-<β-Oxo-propyloxy>-4--2-methyl-naphthalin(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-<β-Oxo-propyloxy>-4--2-methyl-naphthalin(24615-03-0)
    11. EPA Substance Registry System: 1-<β-Oxo-propyloxy>-4--2-methyl-naphthalin(24615-03-0)

  • 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: 24615-03-0(Hazardous Substances Data)

24615-03-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 24615-03-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,6,1 and 5 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 24615-03:
(7*2)+(6*4)+(5*6)+(4*1)+(3*5)+(2*0)+(1*3)=90
90 % 10 = 0
So 24615-03-0 is a valid CAS Registry Number.

24615-03-0Relevant articles and documents

Synthesis and evaluation of mansonone F derivatives as topoisomerase inhibitors

Wu, Wei-Bin,Ou, Jie-Bin,Huang, Zhi-Hong,Chen, Shuo-Bin,Ou, Tian-Miao,Tan, Jia-Heng,Li, Ding,Shen, Liu-Lan,Huang, Shi-Liang,Gu, Lian-Quan,Huang, Zhi-Shu

, p. 3339 - 3347 (2011)

A series of mansonone F (MF) derivatives were designed and synthesized. These compounds were found to be strong inhibitors for topoisomerases, with much more significant inhibition for topoisomerase II rather than topoisomerase I. The best inhibitor showe

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