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CAS

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1393743-23-1

(E)-3-(3-bromophenyl)-1-phenylallyl acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1393743-23-1 Structure

  • Basic information

    1. Product Name: (E)-3-(3-bromophenyl)-1-phenylallyl acetate
    2. Synonyms: (E)-3-(3-bromophenyl)-1-phenylallyl acetate
    3. CAS NO:1393743-23-1
    4. Molecular Formula:
    5. Molecular Weight: 331.209
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1393743-23-1.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)-3-(3-bromophenyl)-1-phenylallyl acetate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (E)-3-(3-bromophenyl)-1-phenylallyl acetate(1393743-23-1)
    11. EPA Substance Registry System: (E)-3-(3-bromophenyl)-1-phenylallyl acetate(1393743-23-1)

  • 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: 1393743-23-1(Hazardous Substances Data)

1393743-23-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1393743-23-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,9,3,7,4 and 3 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1393743-23:
(9*1)+(8*3)+(7*9)+(6*3)+(5*7)+(4*4)+(3*3)+(2*2)+(1*3)=181
181 % 10 = 1
So 1393743-23-1 is a valid CAS Registry Number.

1393743-23-1Relevant articles and documents

A simple and efficient method for the allylation of heteroarenes catalyzed by PdCl2

Yuan, Feng-Quan,Sun, Feng-Yi,Han, Fu-She

, p. 6837 - 6842 (2012/08/28)

The PdCl2-catalyzed allylation of heteroarenes is presented. Various heteroarenes including O-, N-, and S-based ones were allylated efficiently with a rich range of allylic acetates in the presence of only 2 mol % of PdCl2, without the need of bases/acids, additives, and external supporting ligands. In addition, the reactions were carried out under mild and simple conditions just by stirring the two reactants and catalyst in CH 2Cl2 at 60 °C. Moreover, the by-product produced was non-toxic acetic acid. Thus, the method presented in this work provides a general, clean, and operationally simple approach for the functionalization of heteroarenes. Finally, a preliminary mechanistic study suggested that the Pd(II) may be reduced in situ by the heteroarenes to Pd(0), which serves as the active metal center to catalyze the following allylations of heteroarenes via a Tsuji-Trost pathway.

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