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CAS

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30627-64-6

cis-1-ethyl-2-phenylcyclopropane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 30627-64-6 Structure

  • Basic information

    1. Product Name: cis-1-ethyl-2-phenylcyclopropane
    2. Synonyms:
    3. CAS NO:30627-64-6
    4. Molecular Formula:
    5. Molecular Weight: 146.232
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 30627-64-6.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: cis-1-ethyl-2-phenylcyclopropane(CAS DataBase Reference)
    10. NIST Chemistry Reference: cis-1-ethyl-2-phenylcyclopropane(30627-64-6)
    11. EPA Substance Registry System: cis-1-ethyl-2-phenylcyclopropane(30627-64-6)

  • 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: 30627-64-6(Hazardous Substances Data)

30627-64-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 30627-64-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,6,2 and 7 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 30627-64:
(7*3)+(6*0)+(5*6)+(4*2)+(3*7)+(2*6)+(1*4)=96
96 % 10 = 6
So 30627-64-6 is a valid CAS Registry Number.

30627-64-6Relevant articles and documents

Stereoselective Carbon-Carbon Bond-Forming Reaction of 1,1-Dibromocyclopropanes via 1-Halocyclopropylzincates

Harada, Toshiro,Katsuhira, Takeshi,Hattori, Kazuhiro,Oku, Akira

, p. 2958 - 2965 (2007/10/02)

Lithium trialkylzincates react efficiently with 1,1-dibromocyclopropanes 5 to give the corresponding alkylation products 7 nonstereoselectively.The reaction proceeds through a 1,2-alkyl migration of the intermediately formed zincate carbenoid 3 in an inve

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