113664-29-2

Basic information

• Product Name: (2E)-1-(ethylsulfanyl)but-2-ene
• Synonyms: trans-1-(Ethylthio)-2-butene
• CAS NO: 113664-29-2
• Molecular Formula: C₆H₁₂S
• Molecular Weight: 116.2245
• Mol File: 113664-29-2.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 144.6°C at 760 mmHg
• Flash Point: 32.4°C
• Density: 0.859g/cm³
• Vapor Pressure: 6.35mmHg at 25°C
• Refractive Index: 1.472
• CAS DataBase Reference: (2E)-1-(ethylsulfanyl)but-2-ene(CAS DataBase Reference)
• NIST Chemistry Reference: (2E)-1-(ethylsulfanyl)but-2-ene(113664-29-2)
• EPA Substance Registry System: (2E)-1-(ethylsulfanyl)but-2-ene(113664-29-2)

Safety Data

• Hazardous Substances Data: 113664-29-2(Hazardous Substances Data)

Upstream product

• 4784-77-4 (E)-1-Bromo-2-butene 
• 75-08-1 ethanethiol 
• 35976-82-0 (Z)-1-(ethylthio)-2-butene 
• 99116-24-2 4-(ethylthio)-1-butene 
• 106-99-0 buta-1,3-diene 
• 35686-13-6 ethyl (E)-1-butenyl sulfide 

Downstream Products

• 35686-13-6 ethyl (E)-1-butenyl sulfide 
• 35976-82-0 (Z)-1-(ethylthio)-2-butene 
• 83877-59-2 1-cyclohexyl-4-ethylthio-2-methyl-3-buten-1-ol 

Relevant articles and documents

Structure-Stability Relationships in Vinyl Sulfides. III. Stabilization Caused by Different Alkylthio and Phenylthio Groups Attached to an Olefinic Double Bond

The stabilization energies of different alkylthio and phenylthio groups attached to an olefinic double bond have been evaluated with respect to the energy differences of the isomerization reactions of some unsaturated sulfides, in which the double bond migrates from the β,γ- to the α,β-position.According to these results the stabilization energies (in kJ mol-1) are: MeS 15.6, EtS 14.8, i-PrS 15.7, t-BuS 17.5 and PhS 14.4

Selective Condensation of titanium Reagent with Carbonyl Compounds

titanium reagent generated easily from allyl ethyl sulfides condensed with aldehydes to give erythro-β-hydroxy sulfides in highly regio- and stereoselective manner.In contrast, crotyl ethyl sulfide reacted with aldehydes affording δ-hydroxy vinyl sulfide exclusively.The substitution pattern of the starting sulfide can have a pronounced effect on the selectivity in this condensation reaction, erythro-β-Hydroxy sulfide obtained was transfromed stereoselectively to the trans-vinyloxirane or 1,3-alkadiene.