774594-05-7

Upstream product

• 2402-79-1 2,3,5,6-tetrachloropyridine 
• 100-83-4 meta-hydroxybenzaldehyde 

Downstream Products

• 1394052-32-4 6-amino-3-methyl-4-(3-(3,5,6-trichloropyridin-2-yloxy)phenyl)-2,4-dihydropyrano[2,3-c]pyrazole-5-carbonitrile 
• 1394052-35-7 6-amino-3-methyl-1-phenyl-4-(3-(3,5,6-trichloropyridin-2-yloxy)phenyl)-1,4-dihydropyrano[2,3-c]pyrazole-5-carbonitrile 
• 1295506-47-6 2,3,5-trichloro-6-[3-(5-phenyl-4,5-dihydroisoxazol-3-yl)phenoxy]pyridine 
• 1295506-39-6 3-[(3,5,6-trichloropyridin-2-yl)oxy]benzaldehyde oxime 
• 1256574-99-8 (E)-N'-(3-(3,5,6-trichloropyridin-2-yloxy)benzylidene)benzohydrazide 
• 1256575-00-4 (E)-N'-(3-(3,5,6-trichloropyridin-2-yloxy)benzylidene)-2-bromobenzohydrazide 
• 1256575-04-8 (E)-N'-(3-(3,5,6-trichloropyridin-2-yloxy)benzylidene)-2-bromo-4-nitrobenzohydrazide 
• 1256575-03-7 (E)-N'-(3-(3,5,6-trichloropyridin-2-yloxy)benzylidene)-2-bromo-4-fluorobenzohydrazide 
• 1256575-01-5 (E)-N'-(3-(3,5,6-trichloropyridin-2-yloxy)benzylidene)-2-bromo-5-chlorobenzohydrazide 
• 1256575-02-6 (E)-N'-(3-(3,5,6-trichloropyridin-2-yloxy)benzylidene)-2-bromo-5-methoxybenzohydrazide 
• 774594-13-7 3-(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