CAS 50773-56-3
:Benzaldehyde, 4-hydroxy-3-(phenylmethoxy)-
3-Benzyloxy-4-hydroxybenzaldehyde
CAS:Formula:C14H12O3Purity:%Color and Shape:SolidMolecular weight:228.24333-(Benzyloxy)-4-hydroxybenzaldehyde
CAS:3-(Benzyloxy)-4-hydroxybenzaldehydePurity:≥95%Molecular weight:228.24g/mol3-(BENZYLOXY)-4-HYDROXYBENZALDEHYDE
CAS:Formula:C14H12O3Purity:95+%Color and Shape:SolidMolecular weight:228.2473-Benzyloxy-4-hydroxybenzaldehyde
CAS:Controlled ProductApplications A reactant used in the preparation of PDE4 and PDE7 inhibitors, insulin-like growth-factor-I receptor (IGF-IR) inhibitors and ferulic acid derivatives as xanthine oxidase inhibitors.
References Wang, F. et al.: Nat. Prod. Res., 21, 196 (2007); Mulvihill, M. et al.: Bioorg. Med. Chem. Lett., 17, 1091 (2007)Formula:C14H12O3Color and Shape:NeatMolecular weight:228.243-Benzyloxy-4-hydroxybenzaldehyde
CAS:3-Benzyloxy-4-hydroxybenzaldehyde (3BOHB) is an aromatic compound that is used in the synthesis of aporphines. It can be synthesized by using a Wittig reaction with phenylmagnesium bromide and 3-benzyloxybenzoic acid. This product has been shown to have anticancer activity against breast cancer cells, as well as other cancer cells, in mice and rats. 3BOHB is also biosynthesized by clivia plants, and it is commercially available as a starting material for drug synthesis.
Formula:C14H12O3Purity:Min. 95%Molecular weight:228.24 g/mol




