2-Fluoroethyl phenyl sulfide

Base Information

Chemical Name:2-Fluoroethyl phenyl sulfide
CAS No.:134614-32-7
Molecular Formula:C₈H₉FS
Molecular Weight:156.224
Hs Code.:

Synonyms:2-Fluoroethyl phenyl sulfide

Suppliers and Price of 2-Fluoroethyl phenyl sulfide

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of 2-Fluoroethyl phenyl sulfide

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 2-Fluoroethyl phenyl sulfide

There total 1 articles about 2-Fluoroethyl phenyl sulfide which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 45.0%

: 622-38-8
Ethyl phenyl sulfide

: 134614-32-7
2-Fluoroethyl phenyl sulfide

Guidance literature:: With triethylamine tris(hydrogen fluoride); In tetrahydrofuran; electrolyse, Pt electrodes, anodic potential 3.3 V vs. standard sodium calomel electrode (SSCE), charge passed 6.0 F/mol;
DOI:10.1039/c39910001027

Reference yield:

: 134614-32-7
2-Fluoroethyl phenyl sulfide

: 141964-64-9
((1-fluoroethyl)sulfinyl)benzene

Guidance literature:: With 3-chloro-benzenecarboperoxoic acid; In dichloromethane; at -20 ℃; for 1h; Yield given;
DOI:10.1016/S0040-4039(00)77057-2

Reference yield:

: 134614-32-7
((S)-1-Fluoro-ethylsulfanyl)-benzene

: ((S)-(S)-1-Fluoro-ethanesulfinyl)-benzene

: ((R)-(S)-1-Fluoro-ethanesulfinyl)-benzene

Guidance literature:: With 3-chloro-benzenecarboperoxoic acid; In dichloromethane; at -20 ℃; for 3h; Mechanism; other substrates; t-BuOOH, VO(acac)2 instead of m-CPBA;
DOI:10.1016/0040-4039(91)80359-E