50987-90-1

Upstream product

• 106-46-7 para-dichlorobenzene 
• 107-30-2 chloromethyl methyl ether 
• 19036-27-2 2,5-dichloro-α,α'-dibromo-p-xylene 
• 13799-90-1 2,5-dichloroterephthalic acid 
• 95-72-7 2-chloro-1,4-dimethyl-benzene 
• 106-42-3 para-xylene 
• 2800-99-9 2,5-dichlorobenzene-1,4-dimethanol 
• 1124-05-6 1,4-dichloro-2,5-dimethylbenzene 

Downstream Products

• 56403-43-1 1,4-Bis-(cyanomethyl)-2,5-dichlorbenzol 
• 2800-99-9 2,5-dichlorobenzene-1,4-dimethanol 
• 21004-03-5 2,5-dichloro-7,7,8,8-tetracyano-p-quinodimethane 
• 21004-02-4 Dimethyl α,α,α',α'-Tetracyano-2,5-dichlor-p-phenylendiacetat 
• 5409-85-8 1,4-dichloro-2,5-bis-(2-chloro-ethoxymethyl)-benzene 
• 807630-01-9 1-chloromethyl-4-(n-octylsulfinyl)methyl-2,5-dichlorobenzene 
• 872298-77-6 1,4-dichloro-2,5-bis-(2-hydroxy-ethoxymethyl)-benzene 

Relevant academic research and scientific papers

Synthesis and complete NMR spectral assignment of thiophene-substituted sulfinyl monomers

This paper describes the synthesis of thiophene-substituted sulfinyl monomers. It comprises a four-step reaction by which the thiophene unit is built in via Suzuki coupling. These monomers could be used as building blocks for the preparation of conducting

Electron Acceptor Molecules: New, Expedient Synthesis of Substituted 7,7,8,8-Tetracyano-p-quinodimethane (TCNQ) Derivatives and the X-Ray Crystal Structure of 2,5-Dibromo-TCNQ

A range of TCNQ derivatives, viz. 2,5-dichloro, 2,5-dibromo-, 2,5-dimethoxy-, 2-methoxycarbonyl- and benzo-TCNQ, and 11,11,12,12-tetracyanonaphtho-2,6-quinodimethane (TNAP), have been efficiently synthesised using 2-chlorobenzylthiocyanate as the source o