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714966-72-0

(E)-3-(2-Iodo-4-methoxy-phenyl)-acrylic acid ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 714966-72-0 Structure

  • Basic information

    1. Product Name: (E)-3-(2-Iodo-4-methoxy-phenyl)-acrylic acid ethyl ester
    2. Synonyms: (E)-3-(2-Iodo-4-methoxy-phenyl)-acrylic acid ethyl ester
    3. CAS NO:714966-72-0
    4. Molecular Formula:
    5. Molecular Weight: 332.138
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 714966-72-0.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: (E)-3-(2-Iodo-4-methoxy-phenyl)-acrylic acid ethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: (E)-3-(2-Iodo-4-methoxy-phenyl)-acrylic acid ethyl ester(714966-72-0)
    11. EPA Substance Registry System: (E)-3-(2-Iodo-4-methoxy-phenyl)-acrylic acid ethyl ester(714966-72-0)

  • 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: 714966-72-0(Hazardous Substances Data)

714966-72-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 714966-72-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,1,4,9,6 and 6 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 714966-72:
(8*7)+(7*1)+(6*4)+(5*9)+(4*6)+(3*6)+(2*7)+(1*2)=190
190 % 10 = 0
So 714966-72-0 is a valid CAS Registry Number.

714966-72-0Relevant articles and documents

A new total synthesis of (±)-oestrone

Pattenden, Gerald,Reddy, L. Krishnakanth,Walter, Affo

, p. 4027 - 4030 (2004)

A conceptually new total synthesis of oestrone, based on a novel cascade of radical cyclisations from the iodo aryl vinylcyclopropane 2, via 10, 15, 16 and 17, leading to the intermediate trans,anti,trans-oestradiol derivative 11 in one step, is described. Oxidation of 11, followed by demethylation of the resulting aryl methyl ether 18 then gives (±)-oestrone 1.

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