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CAS

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86223-39-4

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

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  • 86223-39-4 Structure

  • Basic information

    1. Product Name: O-Acetylphenacylglycolate
    2. Synonyms:
    3. CAS NO:86223-39-4
    4. Molecular Formula:
    5. Molecular Weight: 236.224
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 86223-39-4.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: O-Acetylphenacylglycolate(CAS DataBase Reference)
    10. NIST Chemistry Reference: O-Acetylphenacylglycolate(86223-39-4)
    11. EPA Substance Registry System: O-Acetylphenacylglycolate(86223-39-4)

  • 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: 86223-39-4(Hazardous Substances Data)

86223-39-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86223-39-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,2,2 and 3 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 86223-39:
(7*8)+(6*6)+(5*2)+(4*2)+(3*3)+(2*3)+(1*9)=134
134 % 10 = 4
So 86223-39-4 is a valid CAS Registry Number.

86223-39-4Downstream Products

86223-39-4Relevant articles and documents

THE RECTION OF ALDEHYDE ENOL SILYL ETHERS WITH LEAD(IV)ACETATE

Rubottom, George M.,Marrero, Roberto,Gruber, John M.

, p. 861 - 866 (2007/10/02)

The treatment of aldehyde enol silyl ethers 1 with lead(IV)acetate (LTA) using methylene chloride as solvent gives rise to the production of α-acetoxy aldehydes 2 and glycolic ester derivatives 3 or enals 5.Structrural variations in 1 are used to explained the divergent trends.When 1 is treated with LTA/KOAc/AcOH, high yields of the corresponding α-acetoxy aldehydes 2 are obtained with the formation of 3 and 5 being subverted.

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