CAS 4397-53-9
:4-(Benzyloxy)benzaldehyde
- 4-(Benzyloxy)benzaldehyde
- 4-(Phenylmethoxy)benzaldehyde
- Benzaldehyde, 4-(phenylmethoxy)-
- Benzaldehyde, p-(benzyloxy)-
- Nsc 131669
- Nsc 28298
- p-(Benzyloxy)benzaldehyde
4-(Benzyloxy)benzaldehyde
CAS:4-(Benzyloxy)benzaldehydePurity:98%Color and Shape:PowderMolecular weight:212.24388g/mol4-Benzyloxybenzaldehyde
CAS:Formula:C14H12O2Purity:min. 98.0 %(GC)Color and Shape:White to Light yellow powder to crystalMolecular weight:212.254-Benzyloxybenzaldehyde
CAS:Formula:C14H12O2Purity:97%Color and Shape:Light yellow powderMolecular weight:212.2484-Benzyloxybenzaldehyde
CAS:Controlled ProductApplications 4-Benzyloxybenzaldehyde is a position isomer of the adenylyl cyclase activator 2-Benzyloxybenzaldehyde. 4-Benzyloxybenzaldehyde also has much less potent anticancer activity against HL-60 cells that its isomeric counterpart.
References Lin, C. et al.: Bioorg. Med. Chem., 13, 1537 (2005); Chang, C.-Y. et al.: Bioorg. Med. Chem. Lett., 11, 1971 (2001);Formula:C14H12O2Color and Shape:NeatMolecular weight:212.244-Benzyloxybenzaldehyde
CAS:4-Benzyloxybenzaldehyde is a molecule with an aldehyde group and a benzyl alcohol group. It is the most active inhibitor of Candida glabrata among the compounds tested. 4-Benzyloxybenzaldehyde has been shown to inhibit Candida glabrata, Propionibacterium acnes, and Pseudomonas aeruginosa. This compound also inhibits hydrogen chloride production by Candida glabrata in vitro. 4-Benzyloxybenzaldehyde inhibits Candida glabrata by binding to the enzyme hydrogenase at the alpha-subunit's active site to prevent its function.
4-Benzyloxybenzaldehyde has been found to be more potent than benzoic acid in inhibiting candida growth, although less potent than gentamicin or erythromycin.Formula:C14H12O2Purity:Min. 95%Molecular weight:212.24 g/mol






