5616-58-0

Basic information

• Product Name: 2-(2-Phenylethenyl)-1,3-dithiolane
• Synonyms: 2-(2-Phenylethenyl)-1,3-dithiolane;2-(2-Phenylvinyl)-1,3-dithiolane;2-Styryl-1,3-dithiolane
• CAS NO: 5616-58-0
• Molecular Formula: C₁₁H₁₂S₂
• Molecular Weight: 208.34298
• Mol File: 5616-58-0.mol
• Article Data: 43

Chemical Properties

• Boiling Point: 340.8°Cat760mmHg
• Flash Point: 166.1°C
• Appearance: /
• Density: 1.256g/cm³
• Vapor Pressure: 0.000165mmHg at 25°C
• Refractive Index: 1.748
• CAS DataBase Reference: 2-(2-Phenylethenyl)-1,3-dithiolane(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(2-Phenylethenyl)-1,3-dithiolane(5616-58-0)
• EPA Substance Registry System: 2-(2-Phenylethenyl)-1,3-dithiolane(5616-58-0)

Safety Data

• Hazardous Substances Data: 5616-58-0(Hazardous Substances Data)

Usage

Synthesis Reference(s)

Tetrahedron Letters, 35, p. 5717, 1994 DOI: 10.1016/S0040-4039(00)77287-X

InChI:InChI=1/C11H12S2/c1-2-4-10(5-3-1)6-7-11-12-8-9-13-11/h1-7,11H,8-9H2/b7-6+

Upstream product

• 7148-78-9 3,3-diethoxyl-1-phenylprop-1-ene 
• 540-63-6 ethane-1,2-dithiol 
• 104-55-2 3-phenyl-propenal 
• 65225-59-4 2-ethoxy-[1,3]dithiolane 
• 83977-12-2 2-((E)-Styryl)-[1,3]dioxolane 
• 37973-54-9 1,1-diacetoxy-3-phenylprop-2-ene 
• 5663-34-3 2-((E)-Styryl)-[1,3]dioxane 
• 621-82-9 Cinnamic acid 

Downstream Products

• 1940-01-8 [1,2,5,6]tetrathiocane 
• 104-55-2 3-phenyl-propenal 
• 103-65-1 phenylpropane 
• 5653-30-5 2-[1,3]dithiolan-2-ylidene-1-phenyl-ethanone 

Relevant articles and documents

Indium-Catalyzed Reductive Dithioacetalization of Carboxylic Acids with Dithiols: Scope, Limitations, and Application to Oxidative Desulfurization

In this study an InI3-TMDS (1,1,3,3-tetramethyldisiloxane) reducing system effectively catalyzed the reductive dithioacetalization of a variety of aromatic and aliphatic carboxylic acids with 1,2-ethanedithiol or 1,3-propanedithiol leading to the one-pot preparation of either 1,3-dithiolane derivatives or a 1,3-dithiane derivative. Also, the intact indium catalyst continuously catalyzed the subsequent oxidative desulfurization of an in situ formed 1,3-dithiolane derivative, which led to the preparation of the corresponding aldehydes.

Mesoporous sBa-15 silica catalyst functionalized with phenylsulfonic acid groups (SbA-15-ph-So3h) as efficient nanocatalyst for chemoselective thioacetalization of carbonyl compounds

In this research a Nano acidic catalyst was prepared and its efficiency on thioacetalization of carbonyl compounds was examined. For this aim we used modified SBA-15 as support, which have been modified by phenolic and sulfonic acid. SBA-15 is a member of

Efficient thioacetalisation of carbonyl compounds

The thioacetalisation of a variety of heterocyclic, aromatic, and aliphatic carbonyl compounds (1 mmol) with ethane-1,2-dithiol (1 mmol) using silica sulphuric acid (SSA) is presented as an efficient heterogeneous catalyst under mild and solvent-free cond