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153644-99-6

Ethyl 2-bromo-2-methyl-3-fluoro-3-phenylpropionate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 153644-99-6 Structure

  • Basic information

    1. Product Name: Ethyl 2-bromo-2-methyl-3-fluoro-3-phenylpropionate
    2. Synonyms: Ethyl 2-bromo-2-methyl-3-fluoro-3-phenylpropionate
    3. CAS NO:153644-99-6
    4. Molecular Formula:
    5. Molecular Weight: 289.144
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 153644-99-6.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: Ethyl 2-bromo-2-methyl-3-fluoro-3-phenylpropionate(CAS DataBase Reference)
    10. NIST Chemistry Reference: Ethyl 2-bromo-2-methyl-3-fluoro-3-phenylpropionate(153644-99-6)
    11. EPA Substance Registry System: Ethyl 2-bromo-2-methyl-3-fluoro-3-phenylpropionate(153644-99-6)

  • 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: 153644-99-6(Hazardous Substances Data)

153644-99-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 153644-99-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,3,6,4 and 4 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 153644-99:
(8*1)+(7*5)+(6*3)+(5*6)+(4*4)+(3*4)+(2*9)+(1*9)=146
146 % 10 = 6
So 153644-99-6 is a valid CAS Registry Number.

153644-99-6Downstream Products

153644-99-6Relevant articles and documents

Stereoselective Hydrogen Transfer Reactions Involving Acyclic Radicals. Tandem Substituted Tetrahydrofuran Formation and Stereoselective Reduction: Synthesis of the C17-C22 Subunit of Ionomycin

Guindon, Y.,Yoakim, C.,Gorys, V.,Ogilvie, W. W.,Delorme, D.,et al.

, p. 1166 - 1178 (2007/10/02)

The tandem iodoetherification reaction and stereoselective reduction of acyclic redicals has been used in the stereocontrolled synthesis of substituted tetrahydrofurans.Such a tetrahydrofuran intermediate is regioselectively cleaved using Me2BBr to reveal

The effect of polar substituents on the conformation and stereochemistry of enolate radicals

Giese,Damm,Wetterich,Zeitz,Rancourt,Guindon

, p. 5885 - 5888 (2007/10/02)

ESR measurements and AM1 calculations show that ester substituted radicals 2 and 6 prefer conformation A as a result of allylic strain effects. But dipolar repulsion between substituents X and CO2Et In 2 and 6 has a pronounced effect on the con

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