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954232-01-0

C16H16N2O5 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 954232-01-0 Structure

  • Basic information

    1. Product Name: C16H16N2O5
    2. Synonyms: C16H16N2O5
    3. CAS NO:954232-01-0
    4. Molecular Formula:
    5. Molecular Weight: 316.313
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 954232-01-0.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: C16H16N2O5(CAS DataBase Reference)
    10. NIST Chemistry Reference: C16H16N2O5(954232-01-0)
    11. EPA Substance Registry System: C16H16N2O5(954232-01-0)

  • 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: 954232-01-0(Hazardous Substances Data)

954232-01-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 954232-01-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,4,2,3 and 2 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 954232-01:
(8*9)+(7*5)+(6*4)+(5*2)+(4*3)+(3*2)+(2*0)+(1*1)=160
160 % 10 = 0
So 954232-01-0 is a valid CAS Registry Number.

954232-01-0Downstream Products

954232-01-0Relevant articles and documents

Synthesis and biological evaluation of quinoxaline derivatives as tubulin polymerization inhibitors that elevate intracellular ROS and triggers apoptosis via mitochondrial pathway

Qi, Jianguo,Huang, Jing,Zhou, Xiaomin,Luo, Wen,Xie, Jiaxin,Niu, Linqiang,Yan, Zhijie,Luo, Yang,Men, Yuhui,Chen, Yanan,Zhang, Yahong,Wang, Jianhong

, p. 617 - 627 (2019/01/18)

A series of novel quinoxaline derivatives were synthesized and evaluated for their antiproliferative activity in three human cancer cell lines. Compound 12 exhibited the most potent antiproliferative activity with IC50 in the range of 0.19–0.51

NOVEL COMPOUNDS

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Page/Page column 59, (2009/08/14)

The invention relates to novel benzimidazole compounds of formula (I) wherein R1 to R1 are as defined in the specification, pharmaceutically acceptable salts thereof, to pharmaceutical compositions containing them and their use in medicine. In particular, the invention relates to compounds that are agonists of peroxisome proliferators-activated receptorγ (PPARγ).

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