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67869-31-2

3β-benzoyloxy-oleanen-(12)-oic acid-(28)-methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 67869-31-2 Structure

  • Basic information

    1. Product Name: 3β-benzoyloxy-oleanen-(12)-oic acid-(28)-methyl ester
    2. Synonyms: 3β-benzoyloxy-oleanen-(12)-oic acid-(28)-methyl ester
    3. CAS NO:67869-31-2
    4. Molecular Formula:
    5. Molecular Weight: 574.844
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 67869-31-2.mol
    9. Article Data: 2

  • 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: 3β-benzoyloxy-oleanen-(12)-oic acid-(28)-methyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3β-benzoyloxy-oleanen-(12)-oic acid-(28)-methyl ester(67869-31-2)
    11. EPA Substance Registry System: 3β-benzoyloxy-oleanen-(12)-oic acid-(28)-methyl ester(67869-31-2)

  • 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: 67869-31-2(Hazardous Substances Data)

67869-31-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 67869-31-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,8,6 and 9 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 67869-31:
(7*6)+(6*7)+(5*8)+(4*6)+(3*9)+(2*3)+(1*1)=182
182 % 10 = 2
So 67869-31-2 is a valid CAS Registry Number.

67869-31-2Downstream Products

67869-31-2Relevant articles and documents

The invention of radical reactions. Part XXXI. Diphenylsilane: A reagent for deoxygenation of alcohols via their thiocarbonyl derivatives, deamination via isonitriles, and dehalogenation of bromo- and iodo- compounds by radical chain chemistry

Barton, Derek H. R.,Jang, Doo Ok,Jaszberenyi, Joseph Cs.

, p. 7193 - 7214 (2007/10/02)

Various thionocarbonates and xanthates of alcohols and bis-xanthates of vic-diols are readily deoxygenated to the corresponding hydrocarbons or olefins, while bromides and iodides are dehalogenated with diphenylphenylsilane in good yield.

The Invention of Radical Reactions. Part XXI. Simple Methods for the Radical Deoxygenation of Primary Alcohols.

Barton, Derek H. R.,Blundell, Paul,Dorchak, Joseph,Jang, Doo Ok,Jaszberenyi, Joseph Cs.

, p. 8969 - 8984 (2007/10/02)

Novel radical-chain deoxygenations of primary alcohols are described.The alcohols are acylated with the reagents pentafluorophenyl chlorothionoformate, 2,4,6-trichlorophenyl chlorothionoformate and 4-fluorophenyl chlorothionoformate and the intermediate thionocarbonates are deoxygenated with tributyltin hydride, triphenylsilane, diphenylsilane or phenylsilane in high-yielding reactions.Key Words: Thionocarbonates, Tributyltin hydride, Triphenylsilane, Diphenylsilane, Phenylsilane, Radical deoxygenations.

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