159150-89-7

Upstream product

• 1539-42-0 bis[(2-pyridyl)methyl]amine 
• 159150-88-6 8-(bromomethyl)-6-methyl-2-phenyl-2,4-dihydro-1,3-benzodioxine 
• 159150-87-5 (6-methyl-2-phenyl-2,4-dihydro-1,3-benzodioxin-8-yl)methanol 
• 1125-88-8 benzaldehyde dimethyl acetal 
• 91-04-3 2,6-bis(hydroxymethyl)-4-methylphenol 

Downstream Products

• 177034-90-1 2-([bis(2-hydroxybenzyl)amino]methyl)-6-([bis(2-pyridinylmethyl)amino]methyl)-4-methylphenol 
• 195621-22-8 2-(N,N-bis((pyridin-2-yl)methyl)aminomethyl)-6-chloromethyl-4-methylphenol 
• 159150-90-0 2-(N,N-bis(2-pyridinylmethyl)aminomethyl)-6-(hydroxymethyl)-4-methylphenol 

Relevant academic research and scientific papers

A versatile key synthon for the syntheses of ligands potentially suited for the preparation of μ-phenoxo dimetallic complexes with two non equivalent complexation sites

The synthon S, easily prepared in two steps (65% yield) from 2,6-bis(hydroxymethyl)-4-methylphenol, may allow the syntheses of various dinucleating ligands bearing two chemically different coordination environments. The preparation of the dinucleating lig

Effect of coordination dissymmetry on the catalytic activity of manganese catalase mimics

Two mixed-valence Mn(II)Mn(III) complexes, [Mn2L1(OAc)2(H2O)]BPh4·2.5H2O and [Mn2L2(OAc)2]·4H2O, obtained with unsymmetrical N4O2