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93222-33-4

Benzene, [1-(1-phenylcyclohexyl)ethenyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 93222-33-4 Structure

  • Basic information

    1. Product Name: Benzene, [1-(1-phenylcyclohexyl)ethenyl]-
    2. Synonyms:
    3. CAS NO:93222-33-4
    4. Molecular Formula: C20H22
    5. Molecular Weight:
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 93222-33-4.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: Benzene, [1-(1-phenylcyclohexyl)ethenyl]-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzene, [1-(1-phenylcyclohexyl)ethenyl]-(93222-33-4)
    11. EPA Substance Registry System: Benzene, [1-(1-phenylcyclohexyl)ethenyl]-(93222-33-4)

  • 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: 93222-33-4(Hazardous Substances Data)

93222-33-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 93222-33-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,2,2 and 2 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 93222-33:
(7*9)+(6*3)+(5*2)+(4*2)+(3*2)+(2*3)+(1*3)=114
114 % 10 = 4
So 93222-33-4 is a valid CAS Registry Number.

93222-33-4Downstream Products

93222-33-4Relevant articles and documents

Transformation of Carbon-Oxygen into Carbon-Carbon Bonds Mediated by Low-Valent Nickel Species

Wenkert, Ernest,Michelotti, Enrique L.,Swindell, Charles S.,Tingoli, Marco

, p. 4894 - 4899 (1984)

The substitution of alkoxy groups of enol ethers (1-methoxycyclohexenes, 1-methoxy-1-alkenes, and benzofuran) and aryl ethers (methoxynaphthalenes, cresyl methyl ethers, and dimethoxybenzenes) by hydrogen, alkyl groups, and aryl units, through Grignard reactions catalyzed by bis(triphenylphosphine)nickel dichloride or nickel dichloride, is described.The stereochemistry of the new reaction is portrayed, especially in connection with processes involving ring opening of dihydropyrans and dihydrofurans.The reaction has been applied to the synthesis of a termite trail pheromone and the acetate of the Douglas fir beetle aggregation pheromone.

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