49858-45-9

Basic information

• Product Name: Benzene, 1-ethenyl-4-[(phenylthio)methyl]-
• CAS NO: 49858-45-9
• Molecular Formula: C15H14S
• Molecular Weight: 226.342
• Mol File: 49858-45-9.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Benzene, 1-ethenyl-4-[(phenylthio)methyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1-ethenyl-4-[(phenylthio)methyl]-(49858-45-9)
• EPA Substance Registry System: Benzene, 1-ethenyl-4-[(phenylthio)methyl]-(49858-45-9)

Safety Data

• Hazardous Substances Data: 49858-45-9(Hazardous Substances Data)

Upstream product

• 591-50-4 iodobenzene 
• 1592-20-7 4-Vinylbenzyl chloride 
• 930-69-8 sodium thiophenolate 
• 79050-33-2 4-(2-bromoethyl)-1-(bromomethyl)benzene 
• 64268-27-5 p-vinylbenzyltrimethylstannate 
• 931-59-9 benzenesulfenyl chloride 

Relevant articles and documents

Eco-compatible three component strategies for C-S bond formation in thioether and S-aryl-carbamodithioate compounds catalyzed by copper(II) nanoparticles supported on modified AlPO4

One-pot and three components C-S bond formation reactions in thioethers and S-aryl-carbamodithioates have been catalyzed by a copper heterogeneous nano-catalyst supported on modified AlPO4 under different reaction conditions. The above-mentioned nano-catalyst has been characterized by various techniques such as SEM, TEM, AFM, XRD, FT-IR, UV–Vis, CV, BET, TGA, ICP and XPS spectrometry and its particle size was estimated to be between 60–110?nm. Finally, the reusability of the catalyst up to ten cycles without any significant leaching is one of the outstanding properties of the catalyst.

Radical-Anion Nucleophilic Substitution in Vinyl Compounds. Reaction of ω-Bromo-4-phenoxymethylstyrene with Sodium Benezenethiolate

Photoinitiated reaction of ω-bromo-4-phenoxymethylstyrene with sodium benzenethiolate results in formation of products of substitution of both the bromine atom and the phenoxy group. The product composition is well consistent with the radical-anion substi