542-81-4

Basic information

• Product Name: 2-CHLOROETHYL METHYL SULFIDE
• Synonyms: 1-Chloro-2-(methylsulfanyl)ethane;1-Chloro-2-(methylthio)ethane;1-chloro-2-methylsulfanyl-ethane;Ethane, 1-chloro-2-(methylthio)-;Ethane,1-chloro-2-(methylthio)-;Sulfide, 2-chloroethyl methyl;B-CHLOROETHYL METHYL SULFIDE;BETA-CHLOROETHYL METHYL SULFIDE
• CAS NO: 542-81-4
• Molecular Formula: C₃H₇ClS
• Molecular Weight: 110.61
• EINECS: 208-828-6
• Product Categories: Small molecule;Building Blocks;Chemical Synthesis;Organic Building Blocks;Sulfides/Disulfides;Sulfur Compounds
• Mol File: 542-81-4.mol
• Article Data: 9

Chemical Properties

• Boiling Point: 55-56 °C30 mm Hg(lit.)
• Flash Point: 108 °F
• Appearance: /
• Density: 1.11 g/mL at 25 °C(lit.)
• Vapor Pressure: 7.81mmHg at 25°C
• Refractive Index: n20/D 1.496(lit.)
• Storage Temp.: 2-8°C
• BRN: 1731033
• CAS DataBase Reference: 2-CHLOROETHYL METHYL SULFIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-CHLOROETHYL METHYL SULFIDE(542-81-4)
• EPA Substance Registry System: 2-CHLOROETHYL METHYL SULFIDE(542-81-4)

Safety Data

• Hazard Codes: C,T
• Statements: 10-20/22-34-23/24-22-45
• Safety Statements: 26-36/37/39-45-53
• RIDADR: UN 2924 3/PG 3
• WGK Germany: 3
• F: 10-13
• HazardClass: 3.2
• PackingGroup: III
• Hazardous Substances Data: 542-81-4(Hazardous Substances Data)

Usage

Uses

2-Chloroethyl methyl sulfide is a monofunctional chemical analog of sulfur mustard and has been used to study the potential of 2,6-dithiopurine as an antagonist of sulfur mustard.

InChI:InChI=1/C3H7ClS/c1-5-3-2-4/h2-3H2,1H3

Upstream product

• 74-93-1 methylthiol 
• 75-01-4 chloroethylene 
• 5271-38-5 2-methylmercapto-ethanol 
• 5813-48-9 Methanesulfenyl chloride 
• 74-85-1 ethene 

Downstream Products

• 25059-70-5 2-chloroethyl dimethyl sulfonium iodide 
• 87231-07-0 methyl 3-phenylpropyl sulfide 
• 13119-15-8 methylthiodiphenylphosphine oxide 
• 616862-96-5 1-[2-(methylsulfanyl)ethyl]-1H-pyrrole 
• 20859-51-2 1-(methylthio)-2-(diphenylphosphino)ethane 
• 865854-40-6 1-(2-chloro-6-dimethylamino-4-trifluoromethylphenyl)-3-cyano-5-[N-methyl-N-(2-methylthioethyl)amino]-4-trifluoromethylthiopyrazole 
• 99075-72-6 2-(2-methylsulfanyl-ethoxy)-benzoic acid amide 
• 688736-79-0 benzyl-(2-methylsulfanyl-ethyl)-amine 
• 107524-40-3 benzyl-(2-methylsulfanyl-ethyl)-malonic acid diethyl ester 
• 876505-49-6 (2-methylsulfanyl-ethyl)-phenyl-malonic acid diethyl ester 
• 75908-66-6 4-methylsulfanyl-2-phenyl-butyronitrile 
• 108479-11-4 1-(2-methylsulfanyl-ethyl)-4-phenyl-piperidine-4-carboxylic acid ethyl ester 
• 100795-83-3 5-(2-methylsulfanyl-ethyl)-5-phenyl-barbituric acid 
• 50890-51-2 2-chloroethyl methyl sulfone 

Relevant articles and documents

γ-cui nanocrystals from self-assembled coordination polymers

Step by step: Two stairstep Cu4I4 coordination polymers 1 and 2 have selectively been synthesized by self-assembly of CuI and 1,4-bis(2-methylthioethoxy)benzene. γ-Cul nanocrystals have been prepared by thermal decomposition of the two stairstep Cu4I4 coordination polymers. Crystal transformation from the two polymers to a cubane Cu4I4 coordination polymer 3 has been observed at initial stage of γ-Cul nanocrystal preparation.

Heterocyclic substituted 2-methyl-benzimidazole antiviral agents

The present invention concerns antiviral compounds, their methods of preparation and their compositions, and use in the treatment of viral infections. More particularly, the invention provides heterocyclic substituted 2-methylbenzimidazole derivatives for the treatment of respiratory syncytial virus infection.

Synthesis of rhenium(I) and technetium(I) carbonyl/dithioether ligand complexes bearing 3,17β-estradiol

Tricarbonyldithioethermetal(I) complexes of rhenium and technetium with a pendant 3,17β-estradiol have been synthesized and characterized. The steroid ligand was bound to the metal centre by the two sulfur atoms of a 4,7-dithiaoct-1-ine spacer.