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107820-29-1

1-hexen-2-yl 4-fluorobenzoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 107820-29-1 Structure

  • Basic information

    1. Product Name: 1-hexen-2-yl 4-fluorobenzoate
    2. Synonyms: 1-hexen-2-yl 4-fluorobenzoate
    3. CAS NO:107820-29-1
    4. Molecular Formula:
    5. Molecular Weight: 222.259
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 107820-29-1.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: 1-hexen-2-yl 4-fluorobenzoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-hexen-2-yl 4-fluorobenzoate(107820-29-1)
    11. EPA Substance Registry System: 1-hexen-2-yl 4-fluorobenzoate(107820-29-1)

  • 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: 107820-29-1(Hazardous Substances Data)

107820-29-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 107820-29-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,8,2 and 0 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 107820-29:
(8*1)+(7*0)+(6*7)+(5*8)+(4*2)+(3*0)+(2*2)+(1*9)=111
111 % 10 = 1
So 107820-29-1 is a valid CAS Registry Number.

107820-29-1Downstream Products

107820-29-1Relevant articles and documents

Ruthenium-Catalyzed Selective Addition of Carboxylic Acids to Alkynes.A Novel Synthesis of Enol Esters

Mitsudo, Take-aki,Hori, Yoji,Yamakawa, Yasushi,Watanabe, Yoshihisa

, p. 2230 - 2239 (1987)

Carboxylic acids react with alkynes in the presence of a catalytic amount of bis(ν5-cyclooctadienyl)ruthenium/trialkylphosphine/maleic anhydride in toluene at 60-80 deg.C to give enol esters having a terminal methylene group in good to excellent yields with high regioselectivity.The deuterium distributions in the products of the reaction of acetic acid-d with 1-hexyne and ethyl propargyl carbonate were examined.Kinetic measurments revealed that the rate has first-order dependence on carboxylic acid, alkyne, and the initial concentration of the ruthenium catalyst.

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