423151-49-9

Upstream product

• 102-47-6 3,4-Dichlorophenylmethyl chloride 
• 121-33-5 vanillin 
• 139-85-5 3,4-dihydroxybenzaldehyde 
• 74-88-4 methyl iodide 

Downstream Products

• 880809-37-0 N-(4-(3,4-dichlorobenzyloxy)-3-methoxybenzyl)-1-(pyridin-4-yl)methanamine 

Relevant academic research and scientific papers

Selected michael additions to thiophene-containing analogues of chalcone

Using thiophene-containing analogues of chalcone as substrates, a series of Michael additions were investigated. Thia-Michael addition of 4-chlorothiophenol led to 1-(substituted aryl)-3-(4-chlorophenylmercapto)-1-(2-thienyl)-1-propanones, whereas catalyt

Vanillin-derived antiproliferative compounds influence Plk1 activity

We synthesized a series of vanillin-derived compounds and analyzed them in HeLa cells for their effects on the proliferation of cancer cells. The molecules are derivatives of the lead compound SBE13, a potent inhibitor of the inactive conformation of huma

Regioselective protection of the 4-hydroxyl of 3,4-dihydroxy-benzaldehyde

The regioselective protection of the 4-hydroxyl group of 3,4-dihydroxy-benzaldehyde was accomplished with seven different protecting groups (benzyl, p-methoxybenzyl, o-nitrobenzyl, 2,6-dichlorobenzyl, 3,4-dichlorobenzyl, vinyl and propargyl) in yields ranging between 67-75percent.