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1284211-16-0

ethyl 3-phenylpropyl phosphite is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1284211-16-0 Structure

  • Basic information

    1. Product Name: ethyl 3-phenylpropyl phosphite
    2. Synonyms:
    3. CAS NO:1284211-16-0
    4. Molecular Formula:
    5. Molecular Weight: 228.228
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1284211-16-0.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: ethyl 3-phenylpropyl phosphite(CAS DataBase Reference)
    10. NIST Chemistry Reference: ethyl 3-phenylpropyl phosphite(1284211-16-0)
    11. EPA Substance Registry System: ethyl 3-phenylpropyl phosphite(1284211-16-0)

  • 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: 1284211-16-0(Hazardous Substances Data)

1284211-16-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1284211-16-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,8,4,2,1 and 1 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1284211-16:
(9*1)+(8*2)+(7*8)+(6*4)+(5*2)+(4*1)+(3*1)+(2*1)+(1*6)=130
130 % 10 = 0
So 1284211-16-0 is a valid CAS Registry Number.

1284211-16-0Downstream Products

1284211-16-0Relevant articles and documents

Direct conversion of benzylic and allylic alcohols to phosphonates

Barney, Rocky J.,Richardson, Rebekah M.,Wiemer, David F.

, p. 2875 - 2879 (2011)

Benzyl phosphonate esters often serve as reagents in Horner-Wadsworth- Emmons reactions. In most cases, they can be prepared from benzylic alcohols via formation of the corresponding halide followed by an Arbuzov reaction. To identify a more direct synthesis of phosphonate esters, we have developed a one-flask procedure for conversion of benzylic and allylic alcohols to the corresponding phosphonates through treatment with triethyl phosphite and ZnI2.

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