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100431-57-0

2',7-dioxotaxol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 100431-57-0 Structure

  • Basic information

    1. Product Name: 2',7-dioxotaxol
    2. Synonyms:
    3. CAS NO:100431-57-0
    4. Molecular Formula:
    5. Molecular Weight: 849.888
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 100431-57-0.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: 2',7-dioxotaxol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2',7-dioxotaxol(100431-57-0)
    11. EPA Substance Registry System: 2',7-dioxotaxol(100431-57-0)

  • 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: 100431-57-0(Hazardous Substances Data)

100431-57-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 100431-57-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,4,3 and 1 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 100431-57:
(8*1)+(7*0)+(6*0)+(5*4)+(4*3)+(3*1)+(2*5)+(1*7)=60
60 % 10 = 0
So 100431-57-0 is a valid CAS Registry Number.

100431-57-0Upstream product

100431-57-0Downstream Products

100431-57-0Relevant articles and documents

Modified Taxols. 2. Oxidation Products of Taxol

Magri, Neal F.,Kingston, David G. I.

, p. 797 - 802 (2007/10/02)

Oxidation of taxol (1) or substituted taxols with Jones' reagent under appropriate conditions yielded 7-oxotaxol (6), 2',7'-dioxotaxol (9), or 2'-oxo-7-acetyltaxol (12).Treatment of 7-oxotaxol with DBU or silica gel yielded a D-secotaxol derivative 14.Hydrogenation of the 2'-acetate derivative of 14 yielded the unstable diketone 16, while hydrogenation of 14 itself followed by workup in methanol gave the lactone 17.

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