77052-33-6

Upstream product

• 17649-94-4 N-phenyl 3-benzoylpropionamide 

Downstream Products

• 104411-91-8 Phenyl-[1-phenyl-5-(phenyl-hydrazono)-4,5-dihydro-1H-pyrazol-3-yl]-methanone 
• 104411-90-7 1-Phenyl-3-benzoyl-5-benzoyloxypyrazole 
• 104411-89-4 1-Phenyl-3-benzoyl-2-pyrazolin-5-one 
• 81470-68-0 3,4-bismethoxycarbonyl-5,N-diphenylphthalimide 
• 81470-70-4 (1S,7R)-2-Benzoyl-3-oxo-4-phenyl-3λ⁴-thia-4-aza-tricyclo[5.2.1.0^2,6]dec-8-en-5-one 
• 81470-67-9 1,3,4-trioxo-2,6-diphenyl-(2H-pyrano<3,4-c>-Δ³-pyrroline) 
• 1027373-19-8 3-(2,6-Dichloro-phenyl)-5-phenyl-3a,6a-dihydro-1-oxa-6-thia-2,5-diaza-pentalen-4-one 
• 1028284-26-5 6a-Benzoyl-3-(2,6-dichloro-phenyl)-5-phenyl-3a,6a-dihydro-1-oxa-6-thia-2,5-diaza-pentalen-4-one 
• 81470-66-8 2-Hydroxy-5-oxo-4-[2-oxo-2-phenyl-eth-(E)-ylidene]-1-phenyl-4,5-dihydro-1H-pyrrole-3-carboxylic acid ethyl ester 
• 81470-65-7 2-hydroxy-3-methoxycarbonyl-4-phenacylidene-1-phenyl-Δ²-pyrrolin-5-one 
• 81470-64-6 5-benzoyl-3-(2,6-dimethylphenylimino)-2-phenylisothiazoline 
• 96252-17-4 2-[2-(2,4-Dinitro-phenyl)-4-phenyl-2H-[1,2,3]thiadiazol-(5Z)-ylidene]-N-phenyl-acetamide 
• 104411-88-3 3-Phenylhydrazono-3-benzoyl-N-phenylpropionamide 
• 81470-62-4 5-benzoyl-2-phenyl-3-phenyliminoisothiazoline 

Relevant academic research and scientific papers

1,3-Dipolar cycloaddition reactions of isothiazol-3(2H)-ones with nitrile oxides. An unexpected site selectivity of the carbonyl bond of 5-benzoyl-isothiazol-3(2H)-one

2,6-Dichlorobenzonitrile oxide (2a) reacts with isothiazolones 1a and 1b at the ethylenic double bond to give 4 via transformation of the primary cycloadducts 3. Mesitonitrile oxide (2b) adds preferentially to the carbonyl double bond of 1b yielding the m

STUDIES ON 5-BENZOYL-3-ISOTHIAZOLINONES

5-Benzoyl-3-isothiazolinones are obtained when β-benzoylpropionamides are heated with thionyl chloride.Some reactions of 5-benzoyl-2-phenyl-3-isothiazolinone are described, the most interesting being that with dimethyl and diethyl malonate carbanions, in

Formation of 5-Aroyl-3-(2H)isothiazolones from the Reaction of 3-Aroylpropionamides with Thionyl Chloride (1)

Reaction of N-substitued-3-aroylpropionamides with excess thionyl chloride was found to give sulfurnitrogen heterocyclic compounds, which were characterized as 2-substituted-5-aroyl-3-(2H)isothiazolones.