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141330-49-6

Cyclohexane, [1-chloro-2-(methylthio)ethyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 141330-49-6 Structure

  • Basic information

    1. Product Name: Cyclohexane, [1-chloro-2-(methylthio)ethyl]-
    2. Synonyms:
    3. CAS NO:141330-49-6
    4. Molecular Formula: C9H17ClS
    5. Molecular Weight: 192.753
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 141330-49-6.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: Cyclohexane, [1-chloro-2-(methylthio)ethyl]-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Cyclohexane, [1-chloro-2-(methylthio)ethyl]-(141330-49-6)
    11. EPA Substance Registry System: Cyclohexane, [1-chloro-2-(methylthio)ethyl]-(141330-49-6)

  • 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: 141330-49-6(Hazardous Substances Data)

141330-49-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 141330-49-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,3,3 and 0 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 141330-49:
(8*1)+(7*4)+(6*1)+(5*3)+(4*3)+(3*0)+(2*4)+(1*9)=86
86 % 10 = 6
So 141330-49-6 is a valid CAS Registry Number.

141330-49-6Downstream Products

141330-49-6Relevant articles and documents

A facile sulfenylchlorination of alkenes with Me2SO/(COCl)2

Lan, Liyuan,Gao, Yang,Ding, Rui,Zhang, Ting,Liu, Yongguo,Sun, Baoguo,Tian, Hongyu

, p. 539 - 549 (2019)

The sulfenylchlorination of a series of alkenes is investigated by using the combined reagent of dimethyl sulfoxide and oxalyl chloride. The corresponding β-chloro sulfides were obtained in mediate to good yields. Most of the terminal alkenes give the Mar

β-Chloroalkyl sulfides from Me2S/SO2Cl2/Me2SO and alkenes

Belessia,Boni,Ghelfi,Pagnoni,Pinetti

, p. 1101 - 1108 (1992)

A novel method to prepare β-chloroalkyl sulfides from alkenes and Me2S-SO2Cl2-Me2SO is described, methanesulfenyl chloride being suggested as intermediate

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