3D-FC112994 - 2-4-chlorobenzyloxybenzaldehyde
2-Benzyloxybenzaldehyde
CAS:Formula:C14H12O2Purity:>98.0%(GC)Color and Shape:Colorless to Yellow clear liquidMolecular weight:212.253-Benzyloxybenzaldehyde
CAS:Formula:C14H12O2Purity:>98.0%(GC)Color and Shape:White to Almost white powder to crystalMolecular weight:212.253-Benzyloxybenzaldehyde, 98%
CAS:3-Benzyloxybenzaldehyde is used as a pharmaceutical intermediate. It activates the adenyl cyclase. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar p
Formula:C14H12O2Purity:98%Color and Shape:Powder, White to creamMolecular weight:212.253-Benzyloxybenzaldehyde
CAS:Formula:C14H12O2Purity:≥ 98.0%Color and Shape:Yellow powderMolecular weight:212.253-Benzyloxybenzaldehyde-α-d1
CAS:Formula:C6H5CH2OC6H4CDOPurity:98 atom % DColor and Shape:White-Tan SolidMolecular weight:213.090014-Benzyloxybenzaldehyde
CAS:Formula:C14H12O2Purity:min. 98.0 %(GC)Color and Shape:White to Light yellow powder to crystalMolecular weight:212.252-Benzyloxybenzaldehyde
CAS:2-Benzyloxybenzaldehyde is an analog of benzaldehyde and can be used as a precursor for the synthesis of other molecules. It has been shown to inhibit the growth of HL-60 cells and xenograft tumor in mice. This compound also inhibits the production of cyclase, which is required to produce prostaglandin E2, a key regulator of inflammation in the body. This inhibition leads to an increase in mitochondrial membrane potential, leading to cell death by apoptosis. 2-Benzyloxybenzaldehyde also inhibits DNA binding activity and has been shown to induce fetal bovine serum levels and colony stimulating factor (CSF) levels in leukemic mice.Formula:C14H12O2Purity:Min. 95%Color and Shape:PowderMolecular weight:212.24 g/mol3-Benzyloxybenzaldehyde
CAS:3-Benzyloxybenzaldehyde (3BOBA) is a hydrochloride salt of 3-benzyloxybenzaldehyde. 3BOBA has shown anti-inflammatory activity in hl-60 cells and prostate cancer cells through inhibition of the activation of nuclear factor kappa B. This inhibition was found to be due to the apoptosis protein, survivin, which was downregulated by 3BOBA treatment. The analogs of 3BOBA are known as curcumin analogs, and have shown anticancer properties in clinical trials.Formula:C14H12O2Purity:Min. 95%Color and Shape:PowderMolecular weight:212.24 g/mol2-Methyl 4-benzyloxybenzaldehyde
CAS:Formula:C15H14O2Purity:96%Color and Shape:SolidMolecular weight:226.2754-Benzyloxybenzaldehyde
CAS:Formula:C14H12O2Purity:97%Color and Shape:Light yellow powderMolecular weight:212.2483-Benzyloxybenzaldehyde
CAS:Formula:C14H12O2Purity:98%Color and Shape:Solid, ChunksMolecular weight:212.2483-Benzyloxybenzaldehyde-α-d1
CAS:Controlled ProductApplications 3-Benzyloxybenzaldehyde-alpha-d1 (CAS# 1219805-34-1) is a useful isotopically labeled research compound.
Formula:C14H11DO2Color and Shape:NeatMolecular weight:213.254-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/mol4-Benzyloxy-3,5-dimethylbenzaldehyde, 95%
CAS:This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Sci
Formula:C16H16O2Purity:95%Color and Shape:Clear yellow, LiquidMolecular weight:240.3Benzaldehyde, 2-methyl-4-(phenylmethoxy)-
CAS:Formula:C15H14O2Purity:96%Color and Shape:SolidMolecular weight:226.2705Benzaldehyde, 3,5-dimethyl-4-(phenylmethoxy)-
CAS:Formula:C16H16O2Purity:97%Color and Shape:SolidMolecular weight:240.2970








