53074-23-0

Basic information

• Product Name: Methanone, phenyl-4-pyridazinyl-
• CAS NO: 53074-23-0
• Molecular Formula: C11H8N2O
• Molecular Weight: 184.197
• Mol File: 53074-23-0.mol
• Article Data: 11

Chemical Properties

• CAS DataBase Reference: Methanone, phenyl-4-pyridazinyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Methanone, phenyl-4-pyridazinyl-(53074-23-0)
• EPA Substance Registry System: Methanone, phenyl-4-pyridazinyl-(53074-23-0)

Safety Data

• Hazardous Substances Data: 53074-23-0(Hazardous Substances Data)

Upstream product

• 289-80-5 1,2-diazine 
• 611-73-4 Benzoylformic acid 
• 103-82-2 phenylacetic acid 
• 53074-22-9 4-benzylpyridazine 
• 140-29-4 phenylacetonitrile 
• 98-88-4 benzoyl chloride 
• 106584-46-7 E,Z-2-benzoyl-5-(benzoyloxy)phenylmethylene-2,5-dihydro-3-pyridazinecarbonitrile 
• 106584-50-3 2-benzoyl-2,3-dihydro-3-pyridazinecarbonitrile 
• 106584-48-9 2-benzoyl-2,3-dihydro-3-pyridazinecarbonitrile 
• 53074-24-1 Phenyl(4-pyridazinyl)methanol 
• 100-52-7 benzaldehyde 
• 74-88-4 methyl iodide 
• 106584-55-8 5-benzoyl-3-pyridazinecarboxylic acid 
• 108-24-7 acetic anhydride 

Downstream Products

• 1163130-41-3 4-methyl-N'-(phenyl(pyridazin-4-yl)methylidene)piperazine-1-carbothiohydrazide 
• 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 
• 1600499-17-9 ethyl 3-phenyl-3-(pyridazin-4-yl)propanoate 
• 96780-96-0 (5-methyl-4-pyridazinyl)phenylmethanone 
• 96780-97-1 (5-methyl-4-pyridazinyl)phenylmethanol 
• 96753-46-7 4-benzyl-5-methylpyridazine 
• 180865-23-0 (E,Z)-Phenyl(4-pyridazinyl)keton-oxim 
• 96780-94-8 1-phenyl-1-(4-pyridazinyl)ethanol 
• 96780-93-7 (2,5-dihydro-5-methyl-4-pyridazinyl)phenylmethanone 
• 139938-17-3 Dimethyl-((Z)-3-phenyl-3-pyridazin-4-yl-allyl)-amine 
• 139938-16-2 Dimethyl-((E)-3-phenyl-3-pyridazin-4-yl-allyl)-amine 

Relevant articles and documents

Ag-catalyzed decarboxylative acylation of pyridazines using α-keto acids in aqueous media

An efficient and general protocol for Ag-Catalyzed decarboxylative acylation of pyridazines using α-keto acids as acylation reagent in aqueous media has been described. This method provides a new avenue for the synthesis of diverse array of acylated pyridazines with different substitution patterns. The reaction proceeds smoothly in water under mild conditions and exhibits a good functional group tolerance.

Benzoyl pyridazine derivative and preparation method thereof

The invention relates to a benzoyl pyridazine derivative and a preparation method thereof, and belongs to the technical field of pyridazine compound synthesis. The benzoyl pyridazine derivative disclosed by the invention has a structure as shown in a form

COMPOUNDS AND METHOD FOR TREATMENT OF CANCER

The invention relates to a compound of Formula (I) and/or a pharmaceutically-acceptable salt, hydrate, solvate, tautomer, optical isomer, E-isomer, Z-isomer, or combination thereof, wherein X is selected from S or O; R5 is selected from a subst