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CAS

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119211-39-1

isopropyl propane-1-thiosulfonate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 119211-39-1 Structure

  • Basic information

    1. Product Name: isopropyl propane-1-thiosulfonate
    2. Synonyms: isopropyl propane-1-thiosulfonate
    3. CAS NO:119211-39-1
    4. Molecular Formula:
    5. Molecular Weight: 182.308
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 119211-39-1.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: isopropyl propane-1-thiosulfonate(CAS DataBase Reference)
    10. NIST Chemistry Reference: isopropyl propane-1-thiosulfonate(119211-39-1)
    11. EPA Substance Registry System: isopropyl propane-1-thiosulfonate(119211-39-1)

  • 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: 119211-39-1(Hazardous Substances Data)

119211-39-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 119211-39-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,2,1 and 1 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 119211-39:
(8*1)+(7*1)+(6*9)+(5*2)+(4*1)+(3*1)+(2*3)+(1*9)=101
101 % 10 = 1
So 119211-39-1 is a valid CAS Registry Number.

119211-39-1Downstream Products

119211-39-1Relevant articles and documents

Palladium-catalysed Hydrosulfination: Synthesis of Sulfonic Acids and S-Alkyl Alkanethiosulfonates from Alkenes, Sulfur Dioxide and Hydrogen

Keim, Wilhelm,Herwig, Juergen

, p. 1592 (1993)

S-Alkyl alkanethiosulfonates and sulfonic acids can easily be synthesized from sulfur dioxide, alkenes, hydrogen and a cationic palladium(II)-diphosphine complex like 2 1 , at temperatures above the ceiling temperature of the SO2-alkene copolymer.

Ultrasound-Accelerated Synthesis of Asymmetrical Thiosulfonate S-Esters by Base-Promoted Reaction of Sulfonyl Chlorides with Thiols

Pham, Hien Thi,Nguyen, Ngoc-Lan Thi,Duus, Fritz,Luu, Thi Xuan Thi

, p. 1934 - 1941 (2015/12/12)

Amberlyst A-26, Mg-Al hydrotalcite, potassium fluoride absorbed on alumina, triethylamine and pyridine have been tested as base catalysts and reagents for the reaction of sulfonyl chlorides with thiols to prepare thiosulfonate S-esters. The reactions were performed under solvent-free conditions or with a minimum amount of solvent assisted by magnetic stirring, ultrasound irradiation and microwave irradiation. Ultrasound irradiation has good effects on the synthesis of sterically hindered thiosulfonate S-esters in solvent-free media as well as in a minimum amount of anhydrous diethyl ether.

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