(Chloromethyl)sulfonylethane

Base Information

• Chemical Name: (Chloromethyl)sulfonylethane
• CAS No.: 1728-94-5
• Molecular Formula: C3H7ClO2S
• Molecular Weight: 142.60448
• European Community (EC) Number: 859-882-8
• Mol file: 1728-94-5.mol

Synonyms:(Chloromethyl)sulfonylethane;1728-94-5;Methane, chloro(ethylsulfonyl)-;1-(chloromethylsulfonyl)ethane;chloromethanesulfonylethane;((chloromethyl)sulfonyl)ethane;SCHEMBL1873868;MFCD19232354;AKOS006384879;AS-60645;CS-0035589;EN300-216048

Chemical Property of (Chloromethyl)sulfonylethane

Chemical Property:

• PSA: 42.52000
• LogP: 1.69820
• XLogP3: 0.7
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 2
• Exact Mass: 141.9855283
• Heavy Atom Count: 7
• Complexity: 120

Purity/Quality:

97% ^*data from raw suppliers

1-(chloromethylsulfonyl)ethane ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCS(=O)(=O)CCl

Technology Process of (Chloromethyl)sulfonylethane

There total 2 articles about (Chloromethyl)sulfonylethane which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

chloromethyl ethyl sulfide (1708-73-2) → Chloromethyl ethyl sulfone (1728-94-5)

Guidance literature:

With Perbenzoic acid; chloroform; at -15 ℃;

Reference yield:

ethylsulfonyl diazomethane (2849-65-2) → Chloromethyl ethyl sulfone (1728-94-5)

Guidance literature:

With hydrogenchloride; In diethyl ether;

Reference yield: 85.0%

Chloromethyl ethyl sulfone (1728-94-5) + benzaldehyde (100-52-7) → 2-Ethanesulfonyl-3-phenyl-oxirane

Guidance literature:

With potassium tert-butylate; In diethyl ether; tert-butyl alcohol; at 20 ℃; for 0.333333h;

DOI:10.1007/BF00955984

upstream raw materials:

chloromethyl ethyl sulfide

ethylsulfonyl diazomethane

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