CAS 50773-56-3
:Benzaldehyde, 4-hydroxy-3-(phenylmethoxy)-
Description:
Benzaldehyde, 4-hydroxy-3-(phenylmethoxy)-, also known by its CAS number 50773-56-3, is an organic compound characterized by its aromatic structure. It features a benzaldehyde moiety with a hydroxyl group and a phenylmethoxy substituent, contributing to its unique chemical properties. This compound typically appears as a colorless to pale yellow liquid with a pleasant aromatic odor. It is soluble in organic solvents such as ethanol and ether but has limited solubility in water due to its hydrophobic aromatic components. The presence of the hydroxyl group imparts some degree of polarity, influencing its reactivity and potential applications. Benzaldehyde derivatives are often utilized in the synthesis of various organic compounds, including pharmaceuticals and fragrances, due to their ability to participate in electrophilic aromatic substitution reactions. Additionally, this compound may exhibit biological activity, making it of interest in medicinal chemistry. Proper handling and storage are essential, as it may pose health risks if inhaled or ingested.
Formula:C14H12O3
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Found 5 products.
3-Benzyloxy-4-hydroxybenzaldehyde
CAS:Formula:C14H12O3Purity:%Color and Shape:SolidMolecular weight:228.24333-(Benzyloxy)-4-hydroxybenzaldehyde
CAS:<p>3-(Benzyloxy)-4-hydroxybenzaldehyde</p>Purity:≥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 Product<p>Applications 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.<br>References Wang, F. et al.: Nat. Prod. Res., 21, 196 (2007); Mulvihill, M. et al.: Bioorg. Med. Chem. Lett., 17, 1091 (2007)<br></p>Formula:C14H12O3Color and Shape:NeatMolecular weight:228.243-Benzyloxy-4-hydroxybenzaldehyde
CAS:<p>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.</p>Formula:C14H12O3Purity:Min. 95%Molecular weight:228.24 g/mol




