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1137728-04-1

diethyl (4-[(t-butyldimethyl)silyloxymethyl]phenyl)methylphosphonate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1137728-04-1 Structure

  • Basic information

    1. Product Name: diethyl (4-[(t-butyldimethyl)silyloxymethyl]phenyl)methylphosphonate
    2. Synonyms: diethyl (4-[(t-butyldimethyl)silyloxymethyl]phenyl)methylphosphonate
    3. CAS NO:1137728-04-1
    4. Molecular Formula:
    5. Molecular Weight: 372.517
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1137728-04-1.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 (4-[(t-butyldimethyl)silyloxymethyl]phenyl)methylphosphonate(CAS DataBase Reference)
    10. NIST Chemistry Reference: diethyl (4-[(t-butyldimethyl)silyloxymethyl]phenyl)methylphosphonate(1137728-04-1)
    11. EPA Substance Registry System: diethyl (4-[(t-butyldimethyl)silyloxymethyl]phenyl)methylphosphonate(1137728-04-1)

  • 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: 1137728-04-1(Hazardous Substances Data)

1137728-04-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1137728-04-1 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 8 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1137728-04:
(9*1)+(8*1)+(7*3)+(6*7)+(5*7)+(4*2)+(3*8)+(2*0)+(1*4)=151
151 % 10 = 1
So 1137728-04-1 is a valid CAS Registry Number.

1137728-04-1Downstream Products

1137728-04-1Relevant articles and documents

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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