85302-11-0

Basic information

• Product Name: (1,5-diphenyl-1H-pyrazol-4-yl)(phenyl)methanone
• Synonyms: (1,5-diphenyl-1H-pyrazol-4-yl)(phenyl)methanone
• CAS NO: 85302-11-0
• Molecular Formula: C₂₂H₁₆N₂O
• Molecular Weight: 324.37524
• Mol File: 85302-11-0.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (1,5-diphenyl-1H-pyrazol-4-yl)(phenyl)methanone(CAS DataBase Reference)
• NIST Chemistry Reference: (1,5-diphenyl-1H-pyrazol-4-yl)(phenyl)methanone(85302-11-0)
• EPA Substance Registry System: (1,5-diphenyl-1H-pyrazol-4-yl)(phenyl)methanone(85302-11-0)

Safety Data

• Hazardous Substances Data: 85302-11-0(Hazardous Substances Data)

Upstream product

• 6831-89-6 1,5-diphenyl-1H-pyrazole 
• 98-88-4 benzoyl chloride 
• 106230-15-3 4-benzoyl-1,5-diphenyl-1H-pyrazole-3-carboxylic acid 
• 85302-05-2 2-((dimethylamino)methylene)-1,3-diphenylpropane-1,3-dione 
• 100-63-0 phenylhydrazine 
• 583-11-9 N-(1-phenylethylidene)phenylhydrazine 
• 17571-17-4 4-benzoyl-5-phenyl-furan-2,3-dione 
• 15397-33-8 3-Oxo-3-phenylpropanal 
• 579-45-3 N-benzoyl-N-phenylhydrazine 
• 57623-20-8 3-benzoyloxy-1-phenyl-propenone 
• 120-46-7 1,3-diphenylpropanedione 
• 574-61-8 benzophenone N-phenylhydrazone 
• 622-73-1 4-methoxybenzaldehydephenylhydrazone 

Downstream Products

• 193747-23-8 (1,5-Diphenyl-1H-pyrazol-4-yl)-phenyl-methanol 

Relevant articles and documents

Synthesis of 4-aroyl-5-arylpyrazoles and 4-aroyl-3-arylpyrazoles via the reaction of enaminodiketones with substituted hydrazines

Pyrazole is a five-membered heterocyclic compound and is one of the important heterocycles in the fields of medicine and pharmacology. Here, we demonstrate the reactivity of symmetrical enaminodiketones 8–14 with substituted hydrazines. When using alkylhy

Reaction of 2-Dimethylaminomethylene-1,3-diones with Dinucleophiles. I. Synthesis of 1,5-Disubstituted 4-Acylpyrazoles

Reaction of open-chain and cyclic sym-1,3-diones with N,N-dimethylformamide dimethyl acetal gave, generally in high yield, a series of sym-2-dimethylaminomethylene-1,3-diones which reacted with phenylhydrazine and methylhydrazine to afford, generally in satisfactory yield, a number of 1,5-disubstituted 4-acylpyrazoles.The applications and limits of this new pyrazole synthesis are presented and discussed.