203631-72-5

Basic information

• Product Name: 1-methylsulfanyl-4-(4-bromophenylsulfanyl)-benzene
• Synonyms: 1-methylsulfanyl-4-(4-bromophenylsulfanyl)-benzene
• CAS NO: 203631-72-5
• Molecular Weight: 311.266
• Mol File: 203631-72-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1-methylsulfanyl-4-(4-bromophenylsulfanyl)-benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-methylsulfanyl-4-(4-bromophenylsulfanyl)-benzene(203631-72-5)
• EPA Substance Registry System: 1-methylsulfanyl-4-(4-bromophenylsulfanyl)-benzene(203631-72-5)

Safety Data

• Hazardous Substances Data: 203631-72-5(Hazardous Substances Data)

Upstream product

• 35371-03-0 4-iodothioanisole 
• 106-53-6 para-bromobenzenethiol 
• 100-68-5 methyl-phenyl-thioether 
• 1192-40-1 copper(I) thiophenolate 
• 104-95-0 (4-bromophenyl)thioanisole 
• 33932-80-8 4-(methylthio)phenyl phenyl sulfide 

Downstream Products

• 203631-80-5 C₂₀H₁₈OS₃ 
• 203631-79-2 C₂₂H₂₂OS₃ 
• 203631-74-7 C₁₉H₁₅BrS₃ 
• 108664-16-0 4-(4-Phenylsulfanyl-phenylsulfanyl)-benzenethiol 
• 203631-76-9 4-[4-(4-Isopropoxy-phenylsulfanyl)-phenylsulfanyl]-benzenethiol 
• 203631-82-7 C₂₈H₂₆OS₄ 
• 203631-78-1 C₁₉H₁₆S₃ 
• 203631-81-6 C₂₅H₂₀S₄ 
• 471866-63-4 4-[4-(4-tert-butoxy-phenylsulfanyl)-phenylsulfanyl]-benzenethiol 
• 471866-62-3 [4-(4-tert-butoxy-phenylsulfanyl)-phenylsulfanyl]-4-methylsulfanyl-benzene 

Relevant articles and documents

Synthesis of molecular chains: phenylene thioether and sulfoxide oligomers

The application of a general synthetic approach to prepare molecular chains is reported. It is based on a step-by-step method each consisting first in a Pd-catalyzed reaction between ArI and HXAr′Br (Ar=aryl, Ar′=arylene) to give ArXAr′Br followed by a Cu

Functionalized p-phenylene sulfides synthesis of new molecular wires

Molecular wires containing p-phenylene sulfide units were synthesized. They could be used in material sciences and in supramolecular chemistry. Wires having 2 to 6 phenyl rings were functionalized at one end by an SH or SMe group, and at the other end, by an OH, OMe or OiPr groups. Formation of Ar-S bonds in the chain was achieved by Pd- or Cu-catalyzed couplings of aromatic thiols with aromatic halides. Conditions for a clean chemoselective deprotection of thiols from thiomethyl groups were developed.