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86047-42-9

ethyl 2-((diphenylphosphoryl)methyl)acrylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 86047-42-9 Structure

  • Basic information

    1. Product Name: ethyl 2-((diphenylphosphoryl)methyl)acrylate
    2. Synonyms: ethyl 2-((diphenylphosphoryl)methyl)acrylate
    3. CAS NO:86047-42-9
    4. Molecular Formula:
    5. Molecular Weight: 314.321
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 86047-42-9.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-((diphenylphosphoryl)methyl)acrylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: ethyl 2-((diphenylphosphoryl)methyl)acrylate(86047-42-9)
    11. EPA Substance Registry System: ethyl 2-((diphenylphosphoryl)methyl)acrylate(86047-42-9)

  • 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: 86047-42-9(Hazardous Substances Data)

86047-42-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86047-42-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,0,4 and 7 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 86047-42:
(7*8)+(6*6)+(5*0)+(4*4)+(3*7)+(2*4)+(1*2)=139
139 % 10 = 9
So 86047-42-9 is a valid CAS Registry Number.

86047-42-9Relevant articles and documents

New accessible ways to 2-ethoxycarbonylallylphosphonates

Mrabet, Hedi,Zantour, Hedi

, p. 25 - 33 (2004)

The Michaelis-Arbusov reaction (method A) and the nucleophilic addition of dialkylphosphites followed by Hoffman olefination (method B) represent two synthetic methods giving a variety of 2-ethoxycarbonylallyl-phosphonates 2, in good yields, from readily accessible ethyl 2-(N,N-dialkylaminomethyl) acrylates 1.

Facile synthesis of bisphosphine monoxides from Morita–Baylis–Hillman carbonates

Zhou, Rong,Zhang, Kai,Liu, Rongfang

, p. 885 - 890 (2016/07/06)

A facile two-step synthesis of bisphosphine monoxides (BPMOs, with both the phosphine and phosphine oxide moieties within one molecule) from readily available Morita–Baylis–Hillman (MBH) carbonates was realized. Under the catalysis of DABCO, the MBH carbo

Synthesis of a functionalized allylic phosphine oxide

Harmata, Michael,Carter, Kevin W.

, p. 3027 - 3033 (2007/10/03)

A functionalized allylic phosphine oxide has been prepared by regioselective bromination of 2-(methyldiphenylphosphinoyl)-1-propene followed by nucleophilic substitution with acetate. Hydrolysis and protection yielded the target compound.

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