Antipsychotics

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Application Conducting polymer precursor. Features and Benefits This bis(bromomethyl)monomer was found to give higher yields of MEH-PPV with higher molecular weights and narrower polydispersities than the corresponding bis(chloromethyl)monomer.

2 5-DIAMINOPHENOL DIHYDROCHLORIDE-

2,5-Dibromothiophene polymerizes by debromination with magnesium catalyzed by nickel compounds to form poly(2,5- thienylene) . Application 2,5-Dibromothiophene was used as starting reagent for the synthesis of &#945,&#945&#8242-didecylquater-,

2,5-Dibromothiophene polymerizes by debromination with magnesium catalyzed by nickel compounds to form poly(2,5- thienylene) . Application 2,5-Dibromothiophene was used as starting reagent for the synthesis of &#945,&#945&#8242-didecylquater-,

1,4-Dichloro-2-nitrobenzene

2,5-Difluorobenzenesulfonamide

2 5-DIFLUOROBENZOIC ACID 98+%

2 6-DICHLOROPYRIDINIUM TETRAFLUOROBORATE

2 6-DICHLOROPYRIDINIUM TETRAFLUOROBORATE

Application 2,6-Difluorobenzonitrile was used in the synthesis of: poly(cyanoaryl ethers) via silyl-method 2-dimethylamino-6-fluorobenzamide phenolphthalein-modified polyarylene ether nitrile copolymers

Application 2,6-Difluorobenzylamine has been used in the synthesis of: ( Z )- N 1 -(2,6-difluorobenzyl)- N 2 -(2-amino-1,2-dicyanovinyl)formamidine 2,6-difluorobenzyl-guanidine hydrochloride