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1137727-99-1

diethyl 2-(4-ethoxycarbonylphenyl)ethylphosphonate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1137727-99-1 Structure

  • Basic information

    1. Product Name: diethyl 2-(4-ethoxycarbonylphenyl)ethylphosphonate
    2. Synonyms: diethyl 2-(4-ethoxycarbonylphenyl)ethylphosphonate
    3. CAS NO:1137727-99-1
    4. Molecular Formula:
    5. Molecular Weight: 314.318
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1137727-99-1.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: diethyl 2-(4-ethoxycarbonylphenyl)ethylphosphonate(CAS DataBase Reference)
    10. NIST Chemistry Reference: diethyl 2-(4-ethoxycarbonylphenyl)ethylphosphonate(1137727-99-1)
    11. EPA Substance Registry System: diethyl 2-(4-ethoxycarbonylphenyl)ethylphosphonate(1137727-99-1)

  • 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: 1137727-99-1(Hazardous Substances Data)

1137727-99-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1137727-99-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,3,7,7,2 and 7 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1137727-99:
(9*1)+(8*1)+(7*3)+(6*7)+(5*7)+(4*2)+(3*7)+(2*9)+(1*9)=171
171 % 10 = 1
So 1137727-99-1 is a valid CAS Registry Number.

1137727-99-1Downstream Products

1137727-99-1Relevant articles and documents

In situ generation of phosphoryl alkylindiums and their synthetic application to arylalkyl phosphonates via palladium-catalyzed cross-coupling reactions

Kim, Sanghyuck,Kim, Cheol-Eui,Seo, Boram,Lee, Phil Ho

, p. 5552 - 5555 (2015/02/19)

Phosphoryl alkylindium reagents are generated in situ from the direct insertion of indium with bromoalkyl phosphonates in the presence of CuCl, and their synthetic application to arylalkyl phosphonates is reported via a Pd-catalyzed cross-coupling reactio

Rh-catalyzed Negishi alkyl-aryl cross-coupling leading to α- or β-phosphoryl-substituted alkylarenes

Takahashi, Hideki,Inagaki, Shinya,Yoshii, Naoko,Gao, Fuxing,Nishihara, Yasushi,Takagi, Kentaro

supporting information; experimental part, p. 2794 - 2797 (2009/09/08)

The catalytic cross-coupling between ArZnX and ICH2(CH 2)nP(O)(OEt)2 (n = 0-3) has been investigated to determine the utility of the Rh catalyst during the alkyl-aryl cross-coupling and to develop a new syntheti

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