27241-60-7

Upstream product

• 3988-77-0 3-phenyl-1-thiophen-2-yl-propenone 
• 3988-77-0 2-cinnamoylthiophene 
• 100-52-7 benzaldehyde 

Downstream Products

• 1093117-00-0 (4,5-dihydro-5-hydroxy-3-phenyl-5-(thiophen-2-yl)pyrazol-1-yl)(pyrrolidin-1-yl)methanethione 
• 1093116-98-3 (4,5-dihydro-5-hydroxy-3-phenyl-5-(thiophen-2-yl)pyrazol-1-yl)(4-methylpiperidin-1-yl)methanethione 
• 1093116-96-1 N-benzyl-4,5-dihydro-5-hydroxy-N-methyl-3-phenyl-5-(thiophen-2-yl)pyrazole-1-carbothioamide 
• 1093116-89-2 4,5-dihydro-5-hydroxy-3-phenyl-5-(thiophen-2-yl)pyrazole-1-carbothioamide 
• 1093117-02-2 N-cyclohexyl-4,5-dihydro-5-hydroxy-3-phenyl-5-(thiophen-2-yl)pyrazole-1-carbothioamide 
• 1093116-90-5 N-adamantyl-4,5-dihydro-5-hydroxy-3-phenyl-5-(thiophen-2-yl)pyrazole-carbothioamide 
• 1093116-94-9 4,5-dihydro-5-hydroxy-3-phenyl5-(thiophen-2-yl)-N-p-tolylpyrazole-1-carbothioamide 
• 1093116-92-7 (4-benzylpiperidin-1-yl)(4,5-dihydro-5-hydroxy-3-phenyl-5-(thiophen-2-yl)pyrazol-1-yl)methanethione 

Relevant academic research and scientific papers

Synthesis and characterization of a new series of hydroxy pyrazolines

3-Phenyl-1-(thiophen-2-yl)prop-2-en-1-one obtained by Claisen-Schmidt condensation of 2-acetyl thiophene with benzaldehyde was converted into 2,3-dibromo-3-phenyl-1-(thiophen-2-yl)propan-1-one, which on treatment with various thiosemicarbazides in the presence of triethylamine in absolute ethanol, yielded the corresponding hydroxy pyrazolines 3a-h. All the compounds were characterized by IR, 1H NMR, and 13C NMR spectra. Copyright Taylor & Francis Group, LLC.