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(Z)-1-Bromo-1-(4-methoxyphenyl)-1-propene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 36233-78-0 Structure
  • Basic information

    1. Product Name: (Z)-1-Bromo-1-(4-methoxyphenyl)-1-propene
    2. Synonyms: (Z)-1-Bromo-1-(4-methoxyphenyl)-1-propene
    3. CAS NO:36233-78-0
    4. Molecular Formula:
    5. Molecular Weight: 227.101
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 36233-78-0.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: (Z)-1-Bromo-1-(4-methoxyphenyl)-1-propene(CAS DataBase Reference)
    10. NIST Chemistry Reference: (Z)-1-Bromo-1-(4-methoxyphenyl)-1-propene(36233-78-0)
    11. EPA Substance Registry System: (Z)-1-Bromo-1-(4-methoxyphenyl)-1-propene(36233-78-0)
  • 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: 36233-78-0(Hazardous Substances Data)

36233-78-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 36233-78-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,2,3 and 3 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 36233-78:
(7*3)+(6*6)+(5*2)+(4*3)+(3*3)+(2*7)+(1*8)=110
110 % 10 = 0
So 36233-78-0 is a valid CAS Registry Number.

36233-78-0Relevant articles and documents

Cycloadditions of 1-(4-Methoxyphenyl)-2-methylvinyl Cation to Olefins. Stereochemistry and Structure of the Reaction Products

Bofinger, Klaus Rainer,Hanack, Michael

, p. 2993 - 3003 (2007/10/02)

(E)-1-Bromo-1-(4-methoxyphenyl)-1-propene (1a) reacts stereospecifically with (Z)-2-butene and silver tetrafluoroborate by cycloaddition of the intermediate vinyl cation 2a to give cis-1-(4-methoxyphenyl)-2,3,4-trimethyl-1-cyclobutene (3); with (E)-2-butene, 3 and trans-1-(4-methoxyphenyl)-2,3,4-trimethyl-1-cyclobutene (4) are formed in a ratio of 1:4.These results are in accord with a synchronous cycloaddition of the vinyl cation 2a to (Z)- and (E)-2-butene.Cyclohexene derivatives 14a, 14b, and 14c are obtained predominantly by the reaction of 1a and AgBF4 or AgSbF6 with vinylcyclopropane (11), ethyl vinyl ether (12), and isobutene (13), respectively.

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