101563-72-8

Basic information

• Product Name: 3(2H)-Pyridazinone, 5-(1-hydroxyethyl)-6-phenyl-
• CAS NO: 101563-72-8
• Molecular Formula: C12H12N2O2
• Molecular Weight: 216.239
• Mol File: 101563-72-8.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 3(2H)-Pyridazinone, 5-(1-hydroxyethyl)-6-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 3(2H)-Pyridazinone, 5-(1-hydroxyethyl)-6-phenyl-(101563-72-8)
• EPA Substance Registry System: 3(2H)-Pyridazinone, 5-(1-hydroxyethyl)-6-phenyl-(101563-72-8)

Safety Data

• Hazardous Substances Data: 101563-72-8(Hazardous Substances Data)

Upstream product

• 404936-89-6 5-acetyl-6-phenyl-2,3-dihydropyridazin-3-one 
• 101563-66-0 6-phenyl-5-hydroxymethyl-2H-pyridazin-3-one 
• 23239-13-6 6-phenyl-5-hydroxymethyl-4,5-dihydro-2H-pyridazin-3-one 
• 101563-68-2 6-oxo-3-phenyl-1,6-dihydropyridazine-4-carbaldehyde 
• 617693-71-7 2-methoxymethyl-6-phenyl-5-[(1'-ethoxy)vinyl]-3-pyridazinone 
• 475084-42-5 1-methoxymethyl-6-oxo-3-phenyl-1,6-dihydropyridazine-4-carbaldehyde 
• 404936-83-0 5-acetyl-2-methoxymethyl-6-phenyl-3(2H)-pyridazinone 
• 90766-97-5 5-bromo-6-phenylpyridazin-3(2H)-one 
• 247158-81-2 2-methoxymethyl-6-phenyl-5-vinyl-3(2H)-pyridazinone 
• 247158-79-8 5-Bromo-2-methoxymethyl-6-phenylpyridazin-3-one 
• 499783-14-1 5-(1'-hydroxyethyl)-2-methoxymethyl-6-phenyl-3(2H)-pyridazinone 
• 101563-80-8 4,5-dihydro-5-(α-hydroxyethyl)-6-phenylpyridazin-3(2H)-one 
• 917-54-4 methyllithium 

Downstream Products

• 404936-89-6 5-acetyl-6-phenyl-2,3-dihydropyridazin-3-one 

Relevant articles and documents

Pyridazine derivatives 32: Stille-based approaches in the synthesis of 5-substituted-6-phenyl-3(2H)-pyridazinones

A series of 6-phenyl-3(2H)-pyridazinones bearing different substituents in the 5-position of the pyridazinone ring were prepared using Stille-based approaches in the search for new platelet-aggregation inhibitors.

Methylation of 5-Aldehydo-6-arylpyridazin-3(2H)-ones via Reaction with Dimethyl and Pentamethyl Cuprates

Me5Cu3Li2 in ether or ether-pentane mixtures, converts the title compounds efficiently into the corresponding 4-methyl derivatives (5) via conjugate methylation of either α,β-unsaturated aldehyde or N=C-C=C system, together with ca. 20percent of 1,2 adduc