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1364569-13-0

ethyl 3,3-difluoro-2-methyl-2-phenylpropanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1364569-13-0 Structure

  • Basic information

    1. Product Name: ethyl 3,3-difluoro-2-methyl-2-phenylpropanoate
    2. Synonyms:
    3. CAS NO:1364569-13-0
    4. Molecular Formula:
    5. Molecular Weight: 228.239
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1364569-13-0.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: ethyl 3,3-difluoro-2-methyl-2-phenylpropanoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: ethyl 3,3-difluoro-2-methyl-2-phenylpropanoate(1364569-13-0)
    11. EPA Substance Registry System: ethyl 3,3-difluoro-2-methyl-2-phenylpropanoate(1364569-13-0)

  • 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: 1364569-13-0(Hazardous Substances Data)

1364569-13-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1364569-13-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,4,5,6 and 9 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1364569-13:
(9*1)+(8*3)+(7*6)+(6*4)+(5*5)+(4*6)+(3*9)+(2*1)+(1*3)=180
180 % 10 = 0
So 1364569-13-0 is a valid CAS Registry Number.

1364569-13-0Downstream Products

1364569-13-0Relevant articles and documents

Umpolung of fluoroform by C-F bond activation: Direct difluoromethylation of lithium enolates

Iida, Toshiaki,Hashimoto, Ryota,Aikawa, Kohsuke,Ito, Shigekazu,Mikami, Koichi

, p. 9535 - 9538 (2012)

Double agent: The direct α-difluoromethylation of lithium enolates using an umpolung form of fluoroform as a difluoromethyl carbocation equivalent leads to an all-carbon quaternary center. Late transition metals are not necessary and the reaction involves activation of inert C-F bonds with subsequent C-C bond formation. Copyright

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