3887-61-4

Upstream product

• 371-42-6 4-Fluorothiophenol 

Downstream Products

• 351-67-7 benzyl-(4-fluorophenyl)-sulfide 
• 328-30-3 2-chlorobenzyl 4-fluorophenyl sulfide 
• 735327-53-4 (2-chloro-benzyl)-(4-chloro-phenyl)-sulfide 
• 19543-85-2 3-(4-fluorophenylthio)propanoic acid 
• 130028-67-0 1,8-bis(4-fluorophenylthio)perfluorooctane 
• 2968-13-0 1-(4-fluoro-phenylsulfanyl)propan-2-one 
• 52673-49-1 4-FC₆H₄SSb(C₆H₅)2 
• 52673-50-4 (C₆H₅)2BiSC₆H₄-p-F 
• 56118-13-9 (4-FC₆H₄)2SbSC₆H₄-4-F 
• 78788-06-4 (CH₃C₆H₄)3SnSC₆H₄F 
• 881171-81-9 4-(4-fluorophenylsulfanyl)-3-hydroxy-2-pyrone 
• 1426-52-4 1-[(4-fluoro-phenylsulfanyl)-methyl]-4-methoxy-benzene 
• 2267-79-0 (2,4-dichloro-benzyl)-(4-fluoro-phenyl)-sulfide 
• 2267-80-3 (2,6-dichloro-benzyl)-(4-fluoro-phenyl)-sulfide 

Relevant academic research and scientific papers

Facile synthesis of mixed O, S or Se bearing hexasubstituted benzenes and their potential as Cu(ii) ion probe

The present study offers a facile route for the synthesis of unsymmetrical hexasubstituted benzenes bearing alternate heteroatoms (O, S and Se) with the formula [1,3,5-(RSeCH2)3-2,4,6-(R′ECH2)3C6] (E

SULPHUR-CONTAINING AND SULPHONATED AROMATIC PERFLUOROALKANE MONOMER

A sulphur-containing and sulphonated aromatic perfluoroalkane monomer is provided that can be used for the manufacture of a polymer membrane for a PEM-type fuel cell. The perfluoroalkane monomer is a functionalized polymer that has a structure correspondi

SULPHUR-CONTAINING TRIAZINE MONOMER THAT CAN BE USED FOR THE SYNTHESIS OF A POLYMER MEMBRANE FOR A FUEL CELL

A sulphur-containing triazine monomer is provided that can be used in the synthesis of a polymer membrane for a PEM-type fuel cell. The sulphur-containing triazine monomer has a structure corresponding to a formula (I): in which: Tz represents a 1,3,5-tri

IMIDATE COMPOUND AND USE THEREOF FOR PEST CONTROL

There is provided a compound having an excellent controlling effect on arthropod pests represented by the formula (I-1): wherein Z represents an optionally substituted carbocyclic group or an optionally substituted heterocyclic group; G represents a -A1-R1

HETEROCYCLIC DIHYDROPYRIMIDINE COMPOUNDS

Novel heterocyclic dihydropyrimidine compounds useful as inhibitors of potassium channel function (especially inhibitors of the Kv1 subfamily of voltage gated K+ channels, especially inhibitors Kv1.5 which has been linked to the ultra rapidly activating d

A process for the preparation and purification of bicalutamide

The invention relates to a process for the preparation of bicalutamide (I) which comprises oxidizing N-[4-cyano-3-(trifluoromethyl)phenyl]-3-[(4-fluorophenyl)thio]-2-hydroxy-2-methyl-propanamide (II) in a solution of peracetic acid in acetic acid and an aromatic solvent. The preparation of (II) from 4-fluorothiophenol and 4-cyano-N-(2,3-epoxy-2-methylpropionyl)-3-trifluoromethylaniline is also disclosed.

Procedure for the synthesis of bicalutamide

The object of the invention is an improved procedure for the synthesis of bicalutamide, characterised in that the 2-hydroxy-2-methyl-3-(4-fluorophenylthio) propionic acid initially produced undergoes a step to acylate the hydroxyl group in position 2 to give an intermediate 2-acyloxy-2-methyl-3-(4-fluorophenylthio) propionic acid, which allows the formation of a successive N-[4-cyano-3-(trifluoromethyl)-phenyl-]-3-[4-fluorophenylthio]-2-acyloxy-2-methyl-propionamide intermediate.