Antipsychotics

2,6-Difluorobenzamide is a major metabolite of pesticide diflubenzuron and has been quantitated by HPLC/diode-array method .

2,6-Difluorobenzamide is a major metabolite of pesticide diflubenzuron and has been quantitated by HPLC/diode-array method .

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

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

2,6-Difluoronitrobenzene is an organic building block. Molecular structure, conformation and potential to internal rotation of 2,6-difluoronitrobenzene been studied by gas-phase electron diffraction (GED), MP2 ab initio, and by B3LYP density

Application 2,6-difluorophenol undergoes oxidative polymerization in the presence of the Fe- N,N&#8242 - bis (salicylidene)ethylenediamine (salen) complex (catalyst) and hydrogen peroxide (oxidizing agent) to give poly(2,6-difluoro-1,4-phenylene

Application 2,6-Difluorophenylboronic acid can be used: As a substrate in the model reaction of Suzuki–Miyaura coupling with&nbsp4-chloro-3-methylanisole. To prepare 4-bromo-2,3&#8242,5&#8242,6-tetrafluorobiphenyl, a key intermediate for the

Application 2,6-Difluorophenylboronic acid can be used: As a substrate in the model reaction of Suzuki–Miyaura coupling with&nbsp4-chloro-3-methylanisole. To prepare 4-bromo-2,3&#8242,5&#8242,6-tetrafluorobiphenyl, a key intermediate for the

Lithium diisopropylamide (LDA)-mediated ortholithiations of 2,6-difluoropyridine in tetrahydrofuran at -78°C has been studied using a combination of IR and NMR spectroscopic and computational methods . Polycondensation of bistrimethylsilyl

Lithium diisopropylamide (LDA)-mediated ortholithiations of 2,6-difluoropyridine in tetrahydrofuran at -78°C has been studied using a combination of IR and NMR spectroscopic and computational methods . Polycondensation of bistrimethylsilyl

2，6-Diiodo-4-(trifluoromethyl)aniline.