5877-11-2

Usage

Uses

Used in Chemical Synthesis:
[(2-chloropropyl)sulfanyl]benzene is used as an intermediate in the chemical synthesis of other organic compounds. Its unique structure allows for further reactions and the creation of a variety of products, contributing to the versatility of [(2-chloropropyl)sulfanyl]benzene in the chemical industry.
Used in Industrial Solvents:
[(2-chloropropyl)sulfanyl]benzene is also employed as a solvent in various industrial processes. Its ability to dissolve a range of substances makes it a valuable asset in the production of different materials and products.
Used in Pharmaceutical Industry:
[(2-chloropropyl)sulfanyl]benzene can be used as a building block for the development of pharmaceutical compounds. Its reactivity and structural properties make it a suitable candidate for the synthesis of new drugs with potential therapeutic applications.
Used in Research and Development:
Due to its unique chemical properties, [(2-chloropropyl)sulfanyl]benzene is also utilized in research and development settings. Scientists and researchers can use [(2-chloropropyl)sulfanyl]benzene to study various chemical reactions and explore its potential applications in creating new materials or improving existing ones.

Upstream product

• 32300-49-5 2-(phenylthio)propan-1-ol 
• 187737-37-7 propene 
• 931-59-9 benzenesulfenyl chloride 
• 64-19-7 acetic acid 
• 937-56-4 1-phenylsulfanyl-propan-2-ol 
• 108-98-5 thiophenol 

Downstream Products

• 5877-16-7 2-(β-phenylsulfanyl-isopropylamino)-ethanol 
• 90696-17-6 3-Methyl-4-phenylsulfanyl-butyric acid ethyl ester 
• 5296-64-0 allyl phenyl thioether 
• 89113-71-3 4-<(phenylthio)methyl>-1-pentene 
• 89113-72-4 5-(phenylthio)-1-hexene 
• 3820-39-1 N_.N-Bis-(phenylmercaptoisopropyl)-2-hydroxy-aethylamin 
• 103153-59-9 2-[benzyl-(β-phenylsulfanyl-isopropyl)-amino]-ethanol 
• 28691-72-7 (E)-1-propenyl phenyl sulfone 
• 3830-06-6 N_.N-Bis-(phenylmercaptoisopropyl)-2-chlor-ethylamin 
• 3830-04-4 N-(Phenylmercaptoisopropyl)-N-benzyl-2-chlor-ethylamin 

Relevant academic research and scientific papers

SUBSTITUTED NICOTINAMIDES AS KCNQ2/3 MODULATORS

The invention relates to substituted nicotinamides, to processes for their preparation, to medicaments comprising these compounds and to the use of these compounds in the preparation of medicaments.

REACTION OF SULFENYL HALIDES WITH ALKENES IN THE PRESENCE OF PERCHLORIC ACID

In the reaction of 2,4-dinitrobenzenesulfenyl chloride and benzenesulfenyl chloride with cyclohexane, propene, and styrene in acetic acid in the presence of perchloric acid the corresponding solvent adducts are formed with yields of 47-75percent.The effect of the perchloric acid on the rate of the reaction of 2,4-dinitrobenzenesulfenyl chloride with cyclohexene is described by an equation for homogeneous catalysis.On the basis of the kinetic data two possible schemes are proposed for the effect of perchloric acid on the formation of the solvent adducts, i.e., a mechanism of homogeneous catalysis and by an ion-exchange mechanism in the noncontrolling stages of the reaction.

O-SILYLATED ENOLATES IN ORGANIC SYNTHESIS: SULPHUR-MEDIATED ALKYLATION OF ESTERS WITH ALKENES.

O-Silylated ester enolates can be alkylated, under ZnBr2-catalysis, by the PhSCl-adducts of mono- and di-substituted alkenes to give γ-phenylthioesters, from which sulphur can be removed both reductively and oxidatively.This alkene carbosulphenylation rea

ALKENE CARBOSULPHENYLATION AND CARBOSELENYLATION: THE USE OF ALLYLTRIMETHYLSILANE AND O-SILYLATED ENOLATES.

Allyltrimethylsilane, as well as O-silylated enolates, can be alkylated by the PhSCl adducts of alkenes and vinyl ethers (1, X=SPh); the PhSeCl analogues (1, X=SePh), however, are less useful for alkylation purposes due to competing nucleophilic attack at selenium.