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CAS

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89986-79-8

Benzeneethanesulfinyl chloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 89986-79-8 Structure

  • Basic information

    1. Product Name: Benzeneethanesulfinyl chloride
    2. Synonyms:
    3. CAS NO:89986-79-8
    4. Molecular Formula: C8H9ClOS
    5. Molecular Weight: 188.678
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 89986-79-8.mol
    9. Article Data: 2

  • 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: Benzeneethanesulfinyl chloride(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzeneethanesulfinyl chloride(89986-79-8)
    11. EPA Substance Registry System: Benzeneethanesulfinyl chloride(89986-79-8)

  • 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: 89986-79-8(Hazardous Substances Data)

89986-79-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89986-79-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,9,8 and 6 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 89986-79:
(7*8)+(6*9)+(5*9)+(4*8)+(3*6)+(2*7)+(1*9)=228
228 % 10 = 8
So 89986-79-8 is a valid CAS Registry Number.

89986-79-8Relevant articles and documents

Direct conversion of sulfinamides to thiosulfonates without the use of additional redox agents under metal-free conditions

Ji, Yuan-Zhao,Li, Hui-Jing,Wang, Jun-Hu,Wu, Yan-Chao,Zhang, Chi

, p. 9291 - 9298 (2021/11/13)

Direct conversion of sulfinamides to thiosulfonates is described. Without the use of additional redox agents, the reaction proceeds smoothly in the presence of TFA under metal-free conditions. This protocol possesses many advantages such as odourless and stable starting materials, broad substrate scope, selective synthesis, and mild reaction conditions. This journal is

Mechanism in the chlorinolysis of sulfinyl chlorides

Ahern, Terence Patrick,Haley, Michael Francis,Langler, Richard Francis,Trenholm, June Ellen

, p. 610 - 614 (2007/10/02)

The successful synthesis and chlorinolysis of α-mercaptodimethyl sulfone have provided additional support for our contention that Pummerer rearrangements may occur during the chlorinolyses of α-sulfonyl sulfinyl chlorides.Further exploration of chlorinolyses of α-sulfonyl systems has uncovered the first observation of CS bond cleavage during the chlorinolyses of (i) a sulfinyl chloride and (ii) a sulfinate ester.

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