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2-chloro-1-(trimethylsilyl)ethyl p-tolyl sulfide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 72610-23-2 Structure
  • Basic information

    1. Product Name: 2-chloro-1-(trimethylsilyl)ethyl p-tolyl sulfide
    2. Synonyms: 2-chloro-1-(trimethylsilyl)ethyl p-tolyl sulfide
    3. CAS NO:72610-23-2
    4. Molecular Formula:
    5. Molecular Weight: 258.887
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 72610-23-2.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: 2-chloro-1-(trimethylsilyl)ethyl p-tolyl sulfide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-chloro-1-(trimethylsilyl)ethyl p-tolyl sulfide(72610-23-2)
    11. EPA Substance Registry System: 2-chloro-1-(trimethylsilyl)ethyl p-tolyl sulfide(72610-23-2)
  • 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: 72610-23-2(Hazardous Substances Data)

72610-23-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 72610-23-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,6,1 and 0 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 72610-23:
(7*7)+(6*2)+(5*6)+(4*1)+(3*0)+(2*2)+(1*3)=102
102 % 10 = 2
So 72610-23-2 is a valid CAS Registry Number.

72610-23-2Upstream product

72610-23-2Downstream Products

72610-23-2Relevant articles and documents

Silicon in Synthesis. 8. Vinyltrimethylsilane, a Convenient Ethylene Equivalent for the Synthesis of Vinyl Aryl Sulfides, Vinyl Aryl Sulfoxides, Thiosilylketene Acetals, and Fused Cyclopentenones

Cooke, Frank,Moerck, Rudi,Schwindeman, James,Magnus, Phillip

, p. 1046 - 1053 (1980)

Vinyltrimethylsilane reacts with a variety of arylsulfenyl chlorides to give 2-chloro-1-(trimethylsilyl)ethyl aryl sulfide adducts 9-13.These adducts can be converted into vinyl aryl sulfides and vinyl aryl sulfoxides, and for the case of 2-chloro-1-(trimethylsilyl)ethyl phenyl sulfide (11), treatment with 1,5-diazabicyclonon-5-ene (DBN) gave 1-(trimethylsilyl)-1-(phenylthio)ethylene (24). α,β-Unsaturated acid chlorides react with vinyltrimethylsilane in the presence of stannic tetrachloride to give fused cyclopentenones.In all of the reaction described, vinyltrimethylsilane serves as a convenient ethylene equivalent.

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