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1032734-49-8

(Z)-2-(2,2-diphenylcyclopropyl)-2-butene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1032734-49-8 Structure

  • Basic information

    1. Product Name: (Z)-2-(2,2-diphenylcyclopropyl)-2-butene
    2. Synonyms:
    3. CAS NO:1032734-49-8
    4. Molecular Formula:
    5. Molecular Weight: 248.368
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1032734-49-8.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: (Z)-2-(2,2-diphenylcyclopropyl)-2-butene(CAS DataBase Reference)
    10. NIST Chemistry Reference: (Z)-2-(2,2-diphenylcyclopropyl)-2-butene(1032734-49-8)
    11. EPA Substance Registry System: (Z)-2-(2,2-diphenylcyclopropyl)-2-butene(1032734-49-8)

  • 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: 1032734-49-8(Hazardous Substances Data)

1032734-49-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1032734-49-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,2,7,3 and 4 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1032734-49:
(9*1)+(8*0)+(7*3)+(6*2)+(5*7)+(4*3)+(3*4)+(2*4)+(1*9)=118
118 % 10 = 8
So 1032734-49-8 is a valid CAS Registry Number.

1032734-49-8Downstream Products

1032734-49-8Relevant articles and documents

The cyclopropyl group as a hypersensitive probe in the singlet oxygen ene reaction mechanism

Alberti, Mariza N.,Orfanopoulos, Michael

, p. 2465 - 2468 (2008)

(Chemical Equation Presented) Cyclopropyl-substituted olefins are employed as mechanistic probes in the singlet oxygen-alkene ene reaction. In MeOH and aprotic solvents [CHCl3, (CH3)2CO, CH 3CN], only the allylic hydroperoxides bearing an intact cyclopropyl group are detected. The reaction mechanism is independent of solvent polarity. Our findings, to a certain experimental limit, exclude a biradical or dipolar intermediate.

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