37032-07-8

Basic information

• Product Name: ETHYL ETHYLTHIOMETHYL SULFOXIDE
• Synonyms: ethyl (ethylthio)methyl sulphoxide;1-[[(Ethylsulfinyl)methyl]thio]ethane
• CAS NO: 37032-07-8
• Molecular Formula: C₅H₁₂OS₂
• Molecular Weight: 152.27818
• EINECS: 253-319-4
• Mol File: 37032-07-8.mol

Chemical Properties

• Boiling Point: 95-100 °C0.1 mm Hg(lit.)
• Flash Point: 125.7°C
• Appearance: /
• Density: 1.112 g/mL at 20 °C(lit.)
• Vapor Pressure: 0.00519mmHg at 25°C
• Refractive Index: n20/D 1.530
• CAS DataBase Reference: ETHYL ETHYLTHIOMETHYL SULFOXIDE(CAS DataBase Reference)
• NIST Chemistry Reference: ETHYL ETHYLTHIOMETHYL SULFOXIDE(37032-07-8)
• EPA Substance Registry System: ETHYL ETHYLTHIOMETHYL SULFOXIDE(37032-07-8)

Safety Data

• Safety Statements: 23-24/25
• WGK Germany: 3
• F: 13
• Hazardous Substances Data: 37032-07-8(Hazardous Substances Data)

Usage

InChI:InChI=1/C5H12OS2/c1-3-7-5-8(6)4-2/h3-5H2,1-2H3

Upstream product

• 109-87-5 Dimethoxymethane 
• 75-08-1 ethanethiol 
• 39213-48-4 ethyl-chloromethyl sulfoxide 
• 4396-19-4 bis(ethylthio)methane 

Downstream Products

• 51760-39-5 1-(Ethanesulfinyl-ethylsulfanyl-methyl)-cyclohexanol 
• 51760-41-9 2-Ethanesulfinyl-2-ethylsulfanyl-1-phenyl-ethanone 
• 49585-43-5 4-bromo-1-ethanesulfinyl-1-ethylsulfanyl-butane 
• 49585-47-9 1-bromo-4-ethanesulfinyl-4-ethylsulfanyl-hexane 

Relevant articles and documents

A convenient and general synthesis of alkyl alkylthiomethyl/aryl arylthiomethyl sulfides and chiral sulfoxides by (camphorsulfonyl)oxaziridines

A convenient efficient procedure for the synthesis of thiomethyl sulfides and their reactions with enantiomerically pure (camphorsulfonyl) oxaziridines results in formation of enantioselective monosulfoxides.

Sulfoxide derivative and process for its preparation

A novel sulfoxide derivative of the general formula STR1 wherein R1 and R3 are the same or different, and each represents and alkyl group having 1 to 4 carbon atoms, a phenyl group or a halo- or methyl-substituted phenyl group, R2 is a hydrogen atom, a lower alkyl group, benzyl group, or a p-methoxy- or p-bromo-benzyl group, R1 and R2, together, may form an alkylene group containing 3 carbon atoms, and X is an oxygen or sulfur atom, and to a process for its preparation.