121137-87-9

Upstream product

• 121137-89-1 4-(2-methoxybenzyl)-6-phenylpyridazine-3(2H)-thione 
• 135-02-4 ortho-anisaldehyde 
• 121137-72-2 4-(2-methoxyphenylmethyl)-6-phenyl-pyridazine-3(2H)-one 
• 1011-46-7 6-phenyl-2,3,4,5-tetrahydropyridazin-3-one 
• 121137-83-5 6-phenyl-4-(2-methoxybenzyl)-3-chloropyridazine 

Downstream Products

• 1155315-88-0 bis{1-[4-(2-methoxybenzyl)-6-phenyl-2H-pyridazin-3-ylidene]-2-butan-2,3-ylidene} hydrazine 
• 1155315-63-1 1-[4-(2-methoxybenzyl)-6-phenyl-2H-pyridazin-3-ylidene]-2-(diphenylmethylene) hydrazine 
• 1155315-13-1 1-[4-(2-methoxybenzyl)-6-phenyl-2H-pyridazin-3-ylidene]-2-(pent-1-ylidene-2,3,4,5-tetraol) hydrazine 
• 1155315-24-4 1-[4-(2-methoxybenzyl)-6-phenyl-2H-pyridazin-3-ylidene]-2-(hexan-1-ylidene-2,3,4,5,6-pentaol) hydrazine 
• 1155314-87-6 C₃₄H₃₀N₄O₄ 
• 1155314-99-0 C₃₆H₃₄N₄O₆ 
• 1155314-69-4 1-[4-(2-methoxybenzyl)-6-phenyl-2H-pyridazin-3-ylidene]-2-(3-methoxy-4-hydroxybenzylidene) hydrazine 
• 1155315-79-9 1-[4-(2-methoxybenzyl)-6-phenyl-2H-pyridazin-3-ylidene]-2-(2-oxo-butan-3-ylidene) hydrazine 
• 1155315-55-1 1-[4-(2-methoxybenzyl)-6-phenyl-2H-pyridazin-3-ylidene]-2-(1-phenylethylidene) hydrazine 
• 1377396-19-4 3-[2-(4-(2-methoxybenzyl)-6-phenylpyridazin-3-yl)hydrazono]-5-methylindolin-2-one 
• 1377396-34-3 3-[2-(4-(2-methoxybenzyl)-6-phenylpyridazin-3-yl)hydrazono]-5-fluoroindolin-2-one 
• 1377396-31-0 3-[2-(4-(2-methoxybenzyl)-6-phenylpyridazin-3-yl)hydrazono]-5-nitroindolin-2-one 
• 1318634-45-5 1-[4-(2-methoxybenzyl)-6-phenylpyridazin-3(2H)-ylidene]-2-acryloylhydrazine 
• 1318634-56-8 N'-[4-(2-methoxybenzyl)-6-phenylpyridazin-3(2H)-ylidene]-2-chloroacetohydrazide 

Relevant academic research and scientific papers

Antiproliferative effects of metal complexes of new isatin hydrazones against HCT116, MCF7 and HELA tumour cell lines

New hydrazone ligands (HL) derived from 5-substituted isatins and 1-(4-(2-methoxybenzyl)-6-arylpyridazin-3-yl)hydrazines and its complexes with Co(II) and Cu(II) were synthesized. The new hydrazones and their complexes were characterized by means of eleme

Reactivity of pyridazin-3(2H) thiones

4,6-Disubstituted pyridazin-3(2H)-thiones 3a-f were prepared by thiation of 4,6-disubstituted pyridazin-3(2H)-one 1a-f either with thiourea or phosphorus pentasulphide. The reactivity of 3a-f towards nucleophilic and electrophilic species under different

SYNTHESIS OF 6-ARYL-4-(o-METHOXYPHENYLMETHYL PYRIDAZINES AND SOME DERIVATIVES

6-Aryl-4,5-dihydro-3(2H)pyridazinones (1a,b) undergo base-catalyzed condensation with o-methoxybenzaldehyde, as an example of deactivated aldehydes, to give 6-aryl-4(o-methoxyphenylmethyl)pyridazin-3(2H)-ones (3a,b) in moderate yields.The reactions of the