Uses
2-Benzyloxy-3-methoxybenzaldehyde (benzyl-
o-vanillin) can be prepared from the reaction of
o-vanillin with benzyl bromide in acetone (solvent) and K
2CO
3 (base) in the presence of tetra-
n-butylammonium iodide (catalyst).
The dihedral angle between the two benzene rings in 2-benzyloxy-3-methoxybenzaldehyde crystal is 23.33 (6)°. Crystal structure suggests that all O atoms are involved in intra and intermolecular C-HO interactions.
It has been reported as key reagent for the synthesis of new anticancer drugs.
It is an important pharmacophore in drug discovery. It exhibits anti-proliferative activity in HL60 leukemia cancer cells.
General Description
2-Benzyloxy-3-methoxybenzaldehyde (benzyl-
o-vanillin) can be prepared from the reaction of
o-vanillin with benzyl bromide in acetone (solvent) and K
2CO
3 (base) in the presence of tetra-
n-butylammonium iodide (catalyst). The dihedral angle between the two benzene rings in 2-benzyloxy-3-methoxybenzaldehyde crystal is 23.33 (6)°. Crystal structure suggests that all O atoms are involved in intra and intermolecular C-HO interactions. It has been reported as key reagent for the synthesis of new anticancer drugs. It is an important pharmacophore in drug discovery. It exhibits anti-proliferative activity in HL60 leukemia cancer cells.
