119887-95-5

Upstream product

• 98-86-2 acetophenone 
• 5499-67-2 5-chloro-1,3-diphenyl-1H-pyrazole-4-carboxaldehyde 
• 4845-49-2 1,3-diphenyl-5-oxo-4,5-dihydro-1H-pyrazole 
• 119887-96-6 (E)-3-(5-Chloro-1,3-diphenyl-1H-pyrazol-4-yl)-1-p-tolyl-propenone 

Downstream Products

• 130088-20-9 1-(5'-Chloro-5,1',3'-triphenyl-3,4-dihydro-1'H-[3,4']bipyrazolyl-2-yl)-ethanone 
• 130088-26-5 5-chloro-4-cyanoacetyl-1,3-diphenyl-1H-pyrazole 
• 130088-18-5 5'-Chloro-5,1',3'-triphenyl-3,4-dihydro-2H,1'H-[3,4']bipyrazolyl 
• 130088-24-3 β-(5-chloro-1,3-diphenyl-1H-pyrazol-4-yl)-β-hydroxylamino-propiophenoneoxime 
• 5499-67-2 5-chloro-1,3-diphenyl-1H-pyrazole-4-carboxaldehyde 
• 36988-06-4 N-(4-methylphenyl)-1,3-diphenyl-1H-pyrazol-5-amine 
• 130088-23-2 5'-Chloro-2,1',3'-triphenyl-5-p-tolyl-3,4-dihydro-2H,1'H-[3,4']bipyrazolyl 
• 130088-21-0 1-(5'-Chloro-1',3'-diphenyl-5-p-tolyl-3,4-dihydro-1'H-[3,4']bipyrazolyl-2-yl)-ethanone 
• 130088-25-4 3-(5-Chloro-1,3-diphenyl-1H-pyrazol-4-yl)-3-hydroxyamino-1-p-tolyl-propan-1-one oxime 
• 130088-29-8 [(E)-3-(5-Chloro-1,3-diphenyl-1H-pyrazol-4-yl)-1-p-tolyl-prop-2-en-(Z)-ylidene]-p-tolyl-amine 
• 130088-19-6 2',5'-Diphenyl-5-p-tolyl-3,4-dihydro-2H,2'H-[3,4']bipyrazolyl-3'-ol 
• 130088-27-6 3-(1,3-diphenyl-5-oxo-1H-pyrazol-4-yl)-1-p-tolylprop-2-en-1-one-oxime 
• 130088-31-2 (E)-3-(5-Methoxy-1,3-diphenyl-1H-pyrazol-4-yl)-1-p-tolyl-propenone 
• 119887-96-6 (E)-3-(5-Chloro-1,3-diphenyl-1H-pyrazol-4-yl)-1-p-tolyl-propenone 

Relevant academic research and scientific papers

SYNTHESIS OF 1-ARYL-3-(5-CHLORO-1,3-DIPHENYL-1H-PYRAZOL-4-YL)PROP-2-EN-1-ONE DERIVATIVES AND THEIR REACTIVITY TOWARD NUCLEOPHILES

1-Aryl-3-(5-chloro-1,3-diphenyl-1H-pyrazol-4-yl)prop-2-en-1-ones 3 were synthesized and made to react with hydrazines, hydroxylamine, p-toluidine, sodium methoxide, alcoholic potassium hydroxide, and aromatic hydrocarbons to give interesting addition prod

FACILE SYNTHESIS OF PYRAZOLOPYRIDINES

The base-catalyzed Michael addition of cyclohexanone, 1,3-diphenyl-2-pyrazolin-5-one, ethyl acetoacetate, and diethyl malonate on 1-aryl-3-(5-chloro-1,3-diphenyl-1H-4-pyrazolyl)-prop-2-en-1-ones (2) in the presence of ammonium acetate at 130 deg C gave th

PECULIAR C-C BOND CLEAVAGES OF PYRAZOLYL PROPENONE EPOXIDES INDUCED BY GRIGNARD REAGENTS.

1-Aryl-3-(5-chloro-1,3-diphenyl-1H-4-pyrazolyl)prop-2-en-1-ones(2) yielded pyrazolylpropenone epoxides (3) on which peculiar C-C bond cleavages were induced by Grignard reagents giving the unexpected saturared secondary alcohols (4) bearing pyrazolyl nucl