642982-66-9

Upstream product

• 2402-79-1 2,3,5,6-tetrachloropyridine 
• 123-08-0 4-hydroxy-benzaldehyde 

Downstream Products

• 1256574-98-7 (E)-N'-(4-(3,5,6-trichloropyridin-2-yloxy)benzylidene)benzohydrazide 
• 1323381-79-8 N-(4-(3,5,6-trichloropyridin-2-yloxy)benzylidene)-2-(4-(3,5,6-trichloropyridin-2-yloxy)phenyl)imidazo[1,2-a]pyridin-3-amine 
• 1394052-30-2 6-amino-3-methyl-4-(4-(3,5,6-trichloropyridin-2-yloxy)phenyl)-2,4-dihydropyrano[2,3-c]pyrazole-5-carbonitrile 
• 1620805-57-3 dimethyl [(phenylamino)({4-[(3,5,6-trichloropyridin-2-yl)oxy]phenyl})methyl]phosphonate 
• 1449036-27-4 5-(2-(1H-indol-3-yl)ethyl)-2-(4-(3,5,6-trichloropyridin-2-yloxy))-1,3,4-oxadiazole 
• 1449036-05-8 N'-(4-(3,5,6-trichloropyridin-2-yloxy)benzylidene)-3-(1H-indol-3-yl)propanehydrazide 
• 1295506-46-5 2,3,5-trichloro-6-[4-(5-phenyl-4,5-dihydroisoxazol-3-yl)phenoxy]pyridine 
• 774594-09-1 4-(3,5,6-trichloro-2-pyridyloxy)phenylmethanol 

Relevant academic research and scientific papers

Synthesis and biological activity of novel 2,5-disubstituted-l,3,4- oxadiazoles

A new and previously unreported molecular framework of 1,3,4-oxadiazoles incorporating halo pyridines has been synthesised. The derivatives are synthesised starting from substituted pyridinyloxy benzaldehydes, by converting them in to corresponding arylidene hydrazides followed by chloramine-T oxidation to the title compounds. The 2,5-disubstituted 1,3,4- oxadiazole derivatives are tested for antimicrobial activity. Many compounds showed high degree of activity against Staphylococus aureus and Escherichia coli bacteria at 250 μg/mL concentration.

ESTER DERIVATIVES OF (PYRIDINYLOXY-PHENYL)-METHANOL AND PROCESS OF PREPARATION THEREOF

The present invention relates to novel pyridinyloxy phenyl methanol derivatives of the formula (III) with X=(a) or (b), obtained by the reaction of 4-/3-(3,5,6-pyridinyl-2-oxy)phenylmethanol and 4-/3-(2,3,5,6-pyridinyl-4-oxy)phenyl methanol with the acid

Oxidative deoximation with catalytic sodium tungstate

A simple and mild method of oxidative deoximation based on catalytic amount of sodium tungstate is described. This method is effective for deprotection of ketones and aldehydes.