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1254063-75-6

O-3-(2-triisopropylsilylethynyl)-2-(methylthio)phenyl N,N-diethylcarbamate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1254063-75-6 Structure

  • Basic information

    1. Product Name: O-3-(2-triisopropylsilylethynyl)-2-(methylthio)phenyl N,N-diethylcarbamate
    2. Synonyms: O-3-(2-triisopropylsilylethynyl)-2-(methylthio)phenyl N,N-diethylcarbamate
    3. CAS NO:1254063-75-6
    4. Molecular Formula:
    5. Molecular Weight: 419.704
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1254063-75-6.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: O-3-(2-triisopropylsilylethynyl)-2-(methylthio)phenyl N,N-diethylcarbamate(CAS DataBase Reference)
    10. NIST Chemistry Reference: O-3-(2-triisopropylsilylethynyl)-2-(methylthio)phenyl N,N-diethylcarbamate(1254063-75-6)
    11. EPA Substance Registry System: O-3-(2-triisopropylsilylethynyl)-2-(methylthio)phenyl N,N-diethylcarbamate(1254063-75-6)

  • 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: 1254063-75-6(Hazardous Substances Data)

1254063-75-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1254063-75-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,4,0,6 and 3 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1254063-75:
(9*1)+(8*2)+(7*5)+(6*4)+(5*0)+(4*6)+(3*3)+(2*7)+(1*5)=136
136 % 10 = 6
So 1254063-75-6 is a valid CAS Registry Number.

1254063-75-6Relevant articles and documents

Synthesis of regioselectively functionalized benzo[b]thiophenes by combined ortho-lithiation-halocyclization strategies

Sanz, Roberto,Guilarte, Veronica,Hernando, Elsa,Sanjuan, Ana M.

, p. 7443 - 7446 (2010)

An efficient synthesis of 3-halo-7-oxygen-functionalized benzo[b]thiophenes bearing different substituents at C-2 has been developed from N,N-diethyl O-3-halophenylcarbamates. The key steps are an ortho-lithiation reaction, which gives rise to 3-halo-2-su

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