4-Benzyloxy-3-methoxybenzaldehyde was used in the synthesis of 1,2-bis(4-benzyloxy-3-methoxyphenyl)-3-hydroxy-propionic acid1. It was also used in first enantioselective total synthesis of a neurotrophic (-)-talaumidin. 4-Benzyloxy-3-methoxybenzaldehyde reacts with benzohydrazide to yield (E)-N?-(4-benzyloxy-3-methoxybenzylidene)benzohydrazide.
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Applications
4-Benzyloxy-3-methoxybenzaldehyde was used in the synthesis of 1,2-bis(4-benzyloxy-3-methoxyphenyl)-3-hydroxy-propionic acid1. It was also used in first enantioselective total synthesis of a neurotrophic (-)-talaumidin. 4-Benzyloxy-3-methoxybenzaldehyde reacts with benzohydrazide to yield (E)-N′-(4-benzyloxy-3-methoxybenzylidene)benzohydrazide.
Solubility
Soluble in chloroform, methanol.
Notes
Air Sensitive. Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Keep away from strong oxidizing agents and strong bases.
RUO – Research Use Only
General References:
- J Shi. (E)-N'-(4-Benzyloxy-3-methoxybenzylidene) isonicotinohydrazide. Acta Crystallographica Section E: Structure Reports. 2005E61 (2), 3933-3934.
- T Hashimoto.; K Hasegawa.; H Yamaguchi.; M Saito. Structure and synthesis of batatasins, dormancy-inducing substances of yam bulbils. Phytochemistry. 197413 (12), 2849-2852.