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1202065-12-0

prop-2-ynyl 4-vinylbenzoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1202065-12-0 Structure

  • Basic information

    1. Product Name: prop-2-ynyl 4-vinylbenzoate
    2. Synonyms: prop-2-ynyl 4-vinylbenzoate
    3. CAS NO:1202065-12-0
    4. Molecular Formula:
    5. Molecular Weight: 186.21
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1202065-12-0.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: prop-2-ynyl 4-vinylbenzoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: prop-2-ynyl 4-vinylbenzoate(1202065-12-0)
    11. EPA Substance Registry System: prop-2-ynyl 4-vinylbenzoate(1202065-12-0)

  • 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: 1202065-12-0(Hazardous Substances Data)

1202065-12-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1202065-12-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,2,0,6 and 5 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1202065-12:
(9*1)+(8*2)+(7*0)+(6*2)+(5*0)+(4*6)+(3*5)+(2*1)+(1*2)=80
80 % 10 = 0
So 1202065-12-0 is a valid CAS Registry Number.

1202065-12-0Downstream Products

1202065-12-0Relevant articles and documents

Oxidative trifluoromethylation of unactivated olefins: An efficient and practical synthesis of α-trifluoromethyl-substituted ketones

Deb, Arghya,Manna, Srimanta,Modak, Atanu,Patra, Tuhin,Maity, Soham,Maiti, Debabrata

, p. 9747 - 9750 (2013)

An economical approach to α-CF3-substituted ketones, which are important intermediates in synthetic and medicinal chemistry, employs olefins and the readily available Langlois reagent (CF3SO 2Na). The reaction is operationally simple, proceeds at room temperature, and exhibits an excellent tolerance toward a wide variety of functional groups. Copyright

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