247158-79-8

Basic information

• Product Name: 3(2H)-Pyridazinone, 5-bromo-2-(methoxymethyl)-6-phenyl-
• CAS NO: 247158-79-8
• Molecular Formula: C12H11BrN2O2
• Molecular Weight: 295.136
• Mol File: 247158-79-8.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 3(2H)-Pyridazinone, 5-bromo-2-(methoxymethyl)-6-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 3(2H)-Pyridazinone, 5-bromo-2-(methoxymethyl)-6-phenyl-(247158-79-8)
• EPA Substance Registry System: 3(2H)-Pyridazinone, 5-bromo-2-(methoxymethyl)-6-phenyl-(247158-79-8)

Safety Data

• Hazardous Substances Data: 247158-79-8(Hazardous Substances Data)

Upstream product

• 107-30-2 chloromethyl methyl ether 
• 90766-97-5 5-bromo-6-phenylpyridazin-3(2H)-one 

Downstream Products

• 247158-83-4 2-Methoxymethyl-6-phenyl-5-(3-hydroxy-1-propinyl)pyridazin-3-one 
• 247158-85-6 2-methoxymethyl-6-phenyl-5-(2-trimethylsilanylethynyl)-3-pyridazinone 
• 351416-08-5 2-methoxymethyl-5,6-diphenyl-2H-pyridazin-3-one 
• 404936-85-2 5-ethynyl-2-methoxymethyl-6-phenyl-3-pyridazinone 
• 562869-98-1 2-methoxymethyl-5-(3-oxo-3-phenylpropenyl)-6-phenyl-3-pyridazinone 
• 562869-99-2 5-(3-hydroxy-3-phenylprop-1-ynyl)-2-methoxymethyl-6-phenyl-3-pyridazinone 
• 247158-80-1 2-Methoxymethyl-6-phenyl-5-styrylpyridazin-3-one 
• 351416-13-2 5-(4-chloro-phenyl)-6-phenyl-2H-pyridazin-3-one 
• 351416-15-4 4-(6-oxo-3-phenyl-1,6-dihydro-pyridazin-4-yl)-benzaldehyde 
• 404936-90-9 6-phenyl-5-(2-trimethylsilanylethynyl)-3(2H)-pyridazinone 

Relevant articles and documents

Pyridazines. Part 28: 5-Alkylidene-6-phenyl-3(2H)-pyridazinones, a new family of platelet aggregation inhibitors

The synthesis and anti-platelet activity of several 5-alkylidene-6-phenyl-3(2H)-pyridazinones are described. The most active compounds are those that contain oxygenated functions (COOR, COMe) on the alkylidene fragment (6a, 6b and 6c).

Pyridazine derivatives. Part 33: Sonogashira approaches in the synthesis of 5-substituted-6-phenyl-3(2H)-pyridazinones

Several 6-phenyl-3(2H)-pyridazinones bearing different alkynyl groups at position 5 have been prepared by a palladium-catalysed Sonogashira cross-coupling reaction. An interesting base-promoted electronically permitted isomerization has been observed duri

Pyridazines. Part 25: Efficient and selective deprotection of pharmacologically useful 2-MOM-pyridazinones using Lewis acids

An efficient and selective procedure for the cleavage of a methoxymethyl group at the 2-position in acid-sensitive pyridazinones is presented. Deprotection with Lewis acids (boron tribromide or aluminium chloride) affords 3(2H)-pyridazinones under mild co