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1224734-13-7

(E)-5-(4-ethoxycarbonylphenyl)-1-phenyl-3-hexene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1224734-13-7 Structure

  • Basic information

    1. Product Name: (E)-5-(4-ethoxycarbonylphenyl)-1-phenyl-3-hexene
    2. Synonyms: (E)-5-(4-ethoxycarbonylphenyl)-1-phenyl-3-hexene
    3. CAS NO:1224734-13-7
    4. Molecular Formula:
    5. Molecular Weight: 308.42
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1224734-13-7.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: (E)-5-(4-ethoxycarbonylphenyl)-1-phenyl-3-hexene(CAS DataBase Reference)
    10. NIST Chemistry Reference: (E)-5-(4-ethoxycarbonylphenyl)-1-phenyl-3-hexene(1224734-13-7)
    11. EPA Substance Registry System: (E)-5-(4-ethoxycarbonylphenyl)-1-phenyl-3-hexene(1224734-13-7)

  • 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: 1224734-13-7(Hazardous Substances Data)

1224734-13-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1224734-13-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,4,7,3 and 4 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1224734-13:
(9*1)+(8*2)+(7*2)+(6*4)+(5*7)+(4*3)+(3*4)+(2*1)+(1*3)=127
127 % 10 = 7
So 1224734-13-7 is a valid CAS Registry Number.

1224734-13-7Downstream Products

1224734-13-7Relevant articles and documents

Copper-catalyzed γ-selective and stereospecific allyl-aryl coupling between (Z)-acyclic and cyclic allylic phosphates and arylboronates

Ohmiya, Hirohisa,Yokokawa, Natsumi,Sawamura, Masaya

supporting information; experimental part, p. 2438 - 2440 (2010/07/10)

A Cu-catalyzed allyl-aryl coupling reaction between (Z)-acyclic or cyclic allylic phosphates and arylboronates proceeds with excellent γ-E-selectivity and 1,3-anti chirality transfer, which gives the corresponding coupling products with benzylic and allylic stereogenic centers. The wide availability and easy-to-handle nature of arylboronates, the inexpensiveness of the Cu catalyst system, and the high regio- and stereoselectivities are attractive features of this protocol.

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