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84785-15-9

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

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  • 84785-15-9 Structure

  • Basic information

    1. Product Name: Acetoxyessigsaeure-acetoxymethylester
    2. Synonyms: Acetoxyessigsaeure-acetoxymethylester
    3. CAS NO:84785-15-9
    4. Molecular Formula:
    5. Molecular Weight: 190.153
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 84785-15-9.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: Acetoxyessigsaeure-acetoxymethylester(CAS DataBase Reference)
    10. NIST Chemistry Reference: Acetoxyessigsaeure-acetoxymethylester(84785-15-9)
    11. EPA Substance Registry System: Acetoxyessigsaeure-acetoxymethylester(84785-15-9)

  • 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: 84785-15-9(Hazardous Substances Data)

84785-15-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84785-15-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,7,8 and 5 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 84785-15:
(7*8)+(6*4)+(5*7)+(4*8)+(3*5)+(2*1)+(1*5)=169
169 % 10 = 9
So 84785-15-9 is a valid CAS Registry Number.

84785-15-9Downstream Products

84785-15-9Relevant articles and documents

Anodic Fragmentation of O-Acylated α-Hydroxy Carboxylic Acids

Thomas, Hans G.,Gabriel, Juergen,Fleischhauer, Joerg,Raabe, Gerhard

, p. 375 - 388 (2007/10/02)

Depending on the degree of substitution at the α-carbon atom, the electrolyses of O-acylated α-hydroxy carboxylic acids 1 yield products of fragmentation (aldehydes or ketones 5) and products derived from acylium ions 4 in concurrence with simple anodic substitution products (acylales, amides, and imides, respectively).Dioxiranyl cations 2 are involved as intermediates.The fragmentation of the dioxiranyl cation 2 is investigated by semiempirical MINDO/3 calculations (Scheme 1).

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