84498-31-7

Upstream product

• 50-00-0 formaldehyd 
• 506-59-2 N,N-dimethylammonium chloride 
• 585-74-0 3-Methylacetophenone 

Downstream Products

• 95605-42-8 Trimethyl-(3-oxo-3-m-tolyl-propyl)-ammonium; bromide 
• 1253195-90-2 1-thiocarbamoyl-3-(3-methylphenyl)-4,5-dihydropyrazole 
• 1253195-98-0 1-(N-methylthiocarbamoyl)-3-(3-methylphenyl)-4,5-dihydropyrazole 
• 1309387-62-9 C₁₆H₁₄BrN₃O 
• 1309387-63-0 3-(1H-benzo[d][1,2,3]triazol-1-yl)-1-oxo-1-m-tolylpropan-2-yl-nicotinate 
• 952286-37-2 C₁₆H₁₅N₃O 
• 228257-33-8 methyl 4-isopropyl-4-m-tolylbutyrate 
• 57494-18-5 4-isopropyl-4-m-tolyl-γ-butyrolactone 
• 160723-51-3 methyl 4-oxo-4-(m-tolyl)butanoate 
• 59618-44-9 4-(3-methylphenyl)-4-oxobutanoic acid 
• 57494-09-4 4-m-Tolyl-5-methylhexansaeure 
• 30543-91-0 litseachromolaevane A 
• 84498-32-8 3-oxo-3-m-tolyl-1-cyanopropane 

Relevant academic research and scientific papers

Stereoselective Construction of γ-Lactams via Copper-Catalyzed Borylacylation

A versatile and highly stereoselective borylative cyclization to generate polyfunctionalized γ-lactams has been developed. The stereoselective synthesis of these key ring systems is crucial due to their ubiquity in natural products. We report the diastero- and enantioselective construction of di- and trisubstituted γ-lactam cores, with examples containing an enantioenriched quaternary carbon.

Synthesis, characterization, crystal structure and DFT studies on 3-(1H-benzo[d][1,2,3]triazol-1-yl)-1-oxo-1-m-tolylpropan-2-yl-nicotinate

3-(1H-Benzo[d][1,2,3]triazol-1-yl)-1-oxo-1-m-tolylpropan-2-yl-nicotinate (BOTN) has been synthesized and characterized by elemental analysis, IR, UV-vis and fluorescence spectroscopy. Its crystal structure has also been determined by X-ray single crystal

Synthesis of new 3-aryl-4,5-dihydropyrazole-1-carbothioamide derivatives. An investigation on their ability to inhibit monoamine oxidase

Some differently substituted 3-aryl-4,5-dihydropyrazoles-1-carbothioamides have been synthesised with the aim to investigate their monoamine oxidase inhibitory activity. The chemical structures of the compounds have been characterized by means of their IR, 1H NMR, 13C NMR spectroscopic data and elemental analyses. All the active compounds showed a selective activity towards the B isoform of the enzyme, regardless of the substitution on the heterocyclic ring. The inhibition of the enzymatic activity was measured on human recombinant MAO isoforms, expressed in baculovirus infected BTI insect cells. Docking experiments were carried out with the aim to rationalize the mechanism of inhibition of the most active and selective compound.