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(E)-1-(trimethylsilyl)-2-(phenylsulfinyl)-ethene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1202351-60-7 Structure
  • Basic information

    1. Product Name: (E)-1-(trimethylsilyl)-2-(phenylsulfinyl)-ethene
    2. Synonyms:
    3. CAS NO:1202351-60-7
    4. Molecular Formula:
    5. Molecular Weight: 224.399
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1202351-60-7.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: (E)-1-(trimethylsilyl)-2-(phenylsulfinyl)-ethene(CAS DataBase Reference)
    10. NIST Chemistry Reference: (E)-1-(trimethylsilyl)-2-(phenylsulfinyl)-ethene(1202351-60-7)
    11. EPA Substance Registry System: (E)-1-(trimethylsilyl)-2-(phenylsulfinyl)-ethene(1202351-60-7)
  • 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: 1202351-60-7(Hazardous Substances Data)

1202351-60-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1202351-60-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,2,3,5 and 1 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1202351-60:
(9*1)+(8*2)+(7*0)+(6*2)+(5*3)+(4*5)+(3*1)+(2*6)+(1*0)=87
87 % 10 = 7
So 1202351-60-7 is a valid CAS Registry Number.

1202351-60-7Downstream Products

1202351-60-7Relevant articles and documents

Addition of sulfenic acids to monosubstituted acetylenes: A theoretical and experimental study

Aversa, Maria Chiara,Barattucci, Anna,Bonaccorsi, Paola,Contini, Alessandro

, p. 1048 - 1057 (2009)

The reaction of benzenesulfenic acid, generated in situ by thermal decomposition of 3-(phenylsulfinyl) propanenitrile, with monosubstituted acetylenes was experimentally and theoretically investigated at the DFT level using the MPW1B95 density functional.

Sulfoxidation of alkenes and alkynes with NFSI as a radical initiator and selective oxidant

Zhang, Yuexia,Wong, Zeng Rong,Wu, Xingxing,Lauw, Sherman J. L.,Huang, Xuan,Webster, Richard D.,Chi, Yonggui Robin

supporting information, p. 184 - 187 (2016/12/27)

Sulfoxides are important functional molecules. We develop a short-route (one-pot) synthesis of this class of molecules by reacting thiols with alkenes or alkynes under mild and metal-free conditions. N-Fluorobenzenesulfonimide (NFSI) is used to play dual roles: as a radical initiator for a thiol-ene/-yne reaction to form sulfide adducts, and as efficient oxidant for conversion of the sulfides formed in situ to sulfoxides. Over-oxidation of the sulfoxides to sulfones is avoided in our approach.

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