129136-45-4

Upstream product

• 622-78-6 Benzyl isothiocyanate 
• 1452-63-7 picolinic acid hydrazide 
• 100-46-9 benzylamine 
• 211572-58-6 N-benzyl-2-picolinoylhydrazinecarbothioamide 
• 3690-47-9 5-mercapto-2-(pyrid-2-yl)-1,3,4-oxadiazole 

Downstream Products

• 359010-75-6 C₁₆H₁₆N₆OS 
• 1352049-63-8 5-[4-benzyl-5-(2-pyridyl)-1,2,4-triazole-3-ylthiomethyl]-1,3,4-oxadiazole-2-thiol 
• 1352049-55-8 1-[(4-benzyl)-5-(2-pyridyl)-4H-1,2,4-triazol-3-ylthiomethylcarboxyl]-3,5-dimethyl-1H-pyrazole 
• 1352049-51-4 2-[-4-benzyl-5-(2-pyridyl)-4H-1,2,4-triazole-3-ylthio]-N⁽²⁾-[1-methyl-3-oxobutilidin]acetohydrazine 
• 257612-58-1 C₁₈H₁₈N₄O₂S 
• 1352049-61-6 (4-benzyl-5-(2-pyridyl)-4H-1,2,4-triazol-3-yl) ethyl sulfide 
• 386746-90-3 N-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-5-(2-pyridyl)-4-benzyl-1,2,4-triazole-2-thione 

Relevant academic research and scientific papers

Synthesis and structure determination of some oxadiazole-2-thione and triazole-3-thione galactosides

The syntheses of 5-pyridyl-3(β-D-galactopyranosyl)-1,3,4-oxadiazole-2-thiones 3a-3c and 5-pyridyl-2(β-D-galactopyranosyl)-4-benzyl-l,2, 4-triazole-3-thiones 6a-6c are reported. The existence of N-galactosides - not S-galactosides - was proven by IR and 15N NMR spectroscopy. The structures of the final products and the intermediates were elucidated by IR, 1H, 13C and 15N NMR spectroscopy and mass spectrometry.

The microwave-assisted dehydrative cyclization of thiosemicarbazides forming substituted 1,2,4-triazoles

Different types of 4,5-disubstituted 1,2,4-triazole-3-thiones were prepared by microwave irradiation as well as by a classical method. The beneficial effect of microwave irradiation on the dehydrative cyclization of thiosemicarbazides in different reactio

Dopamine-beta hydroxylase inhibitors

Dopamine-β-hydroxylase inhibitors of structure: in which R1 is pyridyl or pyridylalkyl, pharmaceutical compositions containing them and their use in therapy in lowering blood pressure.