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1393662-07-1

10-(methylthio)decan-1-yl p-toluenesulfonate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1393662-07-1 Structure

  • Basic information

    1. Product Name: 10-(methylthio)decan-1-yl p-toluenesulfonate
    2. Synonyms: 10-(methylthio)decan-1-yl p-toluenesulfonate
    3. CAS NO:1393662-07-1
    4. Molecular Formula:
    5. Molecular Weight: 358.566
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1393662-07-1.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: 10-(methylthio)decan-1-yl p-toluenesulfonate(CAS DataBase Reference)
    10. NIST Chemistry Reference: 10-(methylthio)decan-1-yl p-toluenesulfonate(1393662-07-1)
    11. EPA Substance Registry System: 10-(methylthio)decan-1-yl p-toluenesulfonate(1393662-07-1)

  • 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: 1393662-07-1(Hazardous Substances Data)

1393662-07-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1393662-07-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,9,3,6,6 and 2 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1393662-07:
(9*1)+(8*3)+(7*9)+(6*3)+(5*6)+(4*6)+(3*2)+(2*0)+(1*7)=181
181 % 10 = 1
So 1393662-07-1 is a valid CAS Registry Number.

1393662-07-1Relevant articles and documents

Efficient Swern oxidation and Corey-Kim oxidation with ion-supported methyl sulfoxides and methyl sulfides

Tsuchiya, Daisuke,Tabata, Masayuki,Moriyama, Katsuhiko,Togo, Hideo

, p. 6849 - 6855 (2012)

The Swern oxidation of various benzylic and allylic alcohols, primary alcohols, and secondary alcohols with two ion-supported methyl sulfoxides A-1 (C6) and B-1 (C10), and oxalyl chloride in the presence of triethylamine in dichloromethane, followed by simple diethyl ether extraction of the reaction mixture, gave the corresponding aldehydes and ketones, respectively, in good yields with high purity. Similarly, the Corey-Kim oxidation of various benzylic and allylic alcohols, primary alcohols, and secondary alcohols with two ion-supported methyl sulfides A-2 (C6) and B-2 (C10), and N-chlorosuccinimide in the presence of triethylamine in dichloromethane, followed by simple diethyl ether extraction of the reaction mixture, furnished the corresponding aldehydes and ketones, respectively, in good yields with high purity. Both reactions did not produce any unpleasant odor at all. In the Swern oxidation, ion-supported methyl sulfides were recovered in high yields and could be re-oxidized to produce ion-supported methyl sulfoxides A-1 (C6) and B-1 (C10), for reuse in the same oxidation. In the Corey-Kim oxidation, ion-supported methyl sulfides A-2 (C6) and B-2 (C10) were recovered in high yields and could be also reused for the same oxidation.

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