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93677-03-3

2-Propenoic acid, 3-(4-iodophenyl)-, Methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 93677-03-3 Structure

  • Basic information

    1. Product Name: 2-Propenoic acid, 3-(4-iodophenyl)-, Methyl ester
    2. Synonyms: 2-Propenoic acid, 3-(4-iodophenyl)-, Methyl ester
    3. CAS NO:93677-03-3
    4. Molecular Formula: C10H9IO2
    5. Molecular Weight: 288.08173
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 93677-03-3.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-Propenoic acid, 3-(4-iodophenyl)-, Methyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Propenoic acid, 3-(4-iodophenyl)-, Methyl ester(93677-03-3)
    11. EPA Substance Registry System: 2-Propenoic acid, 3-(4-iodophenyl)-, Methyl ester(93677-03-3)

  • 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: 93677-03-3(Hazardous Substances Data)

93677-03-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 93677-03-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,6,7 and 7 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 93677-03:
(7*9)+(6*3)+(5*6)+(4*7)+(3*7)+(2*0)+(1*3)=163
163 % 10 = 3
So 93677-03-3 is a valid CAS Registry Number.

93677-03-3Relevant articles and documents

Hydrogen Peroxide Promoted Mizoroki-Heck Reactions of Phenyldiazenes with Acrylates, Acrylamides, and Styrenes

Lasch, Roman,Fehler, Stefanie K.,Heinrich, Markus R.

supporting information, p. 1586 - 1589 (2016/05/02)

Mizoroki-Heck reactions, which are well-known for aryldiazonium salts and which have recently been described for arylhydrazines, have now been extended to phenyldiazenes. In situ generation of phenyldiazenes from azocarboxylates allowed clean and selective reactions with styrenes, acrylates, and acrylamides using palladium(II) acetate in the presence of silver(I) acetate or hydrogen peroxide as oxidant. Hydrogen peroxide was thereby shown to be a cheap and broadly applicable alternative for the established palladium-silver(I) system.

Heck reactions using segmented flow conditions

Ahmed-Omer, Batoul,Barrow, David A.,Wirth, Thomas

experimental part, p. 3352 - 3355 (2009/08/17)

Various Heck couplings have been carried out using segmented flow conditions to accelerate the reactions. Aryl iodides and aryl bromides as well as anilines in diazonium-type Heck reactions have been used successfully.

Total Synthesis of Combretastatin D-2: Intramolecular Ullmann Macrocyclization Reaction

Boger, Dale L.,Sakya, Subas M.,Yohannes, Daniel

, p. 4204 - 4207 (2007/10/02)

The total synthesis of combretastatin D-2, a cytotoxic constituent of Combretum caffrum (Combretaceae), is detailed and is based on the implementation of a key intramolecular Ullmann macrocyclization reaction for formation of the cyclic 15-membered caffra

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