53074-22-9

Basic information

• Product Name: Pyridazine, 4-(phenylmethyl)-
• CAS NO: 53074-22-9
• Molecular Formula: C11H10N2
• Molecular Weight: 170.214
• Mol File: 53074-22-9.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Pyridazine, 4-(phenylmethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Pyridazine, 4-(phenylmethyl)-(53074-22-9)
• EPA Substance Registry System: Pyridazine, 4-(phenylmethyl)-(53074-22-9)

Safety Data

• Hazardous Substances Data: 53074-22-9(Hazardous Substances Data)

Upstream product

• 289-80-5 1,2-diazine 
• 103-82-2 phenylacetic acid 
• 53074-24-1 Phenyl(4-pyridazinyl)methanol 
• 94693-71-7 4-α-Chlorbenzylpyridazin 

Downstream Products

• 53074-23-0 4-Benzoylpyridazine 
• 1600499-17-9 ethyl 3-phenyl-3-(pyridazin-4-yl)propanoate 
• 1600499-18-0 3-phenyl-3-(pyridazin-4-yl)propanoic acid 
• 1600499-19-1 3-phenyl-3-(pyridazin-4-yl)propanoyl azide 
• 1600499-20-4 tert-butyl (2-phenyl-2-(pyridazin-4-yl)ethyl)carbamate 
• 1598429-41-4 2-phenyl-2-(pyridazin-4-yl)ethanamine 

Relevant articles and documents

Benzamides

The present invention is directed to benzamide containing compounds which inhibit the P2X7 receptor

Telesubstitution and Dismutation Reactions in the Series of Phenyl-3-pyridazinylmethane Derivatives

Reactions of 3-α-chlorobenzylpyridazine (4) with alkoxides have been found to yield 6-substituted or 4-substituted 3-benzylpyridazines (7a-c, 8a-c) rather than the usual ethers (6a-c).Introduction of an electron-donating substituent into the 6-position of the pyridazine nucleus of 4 has been shown to suppress such telesubstitution processes.With phenyl-3-pyridazinylmethanol (3), thermally induced dismutation affording 3-benzylpyridazine (17) and 3-benzoylpyridazine (11) has been observed. Key Words: 3-Pyridazinylmethyl chlorides, reactions with O-nucleophiles / Telesubstitution / Dismutation, thermally induced