CAS 952-17-0

(3,4-diethoxyphenyl)(oxo)acetaldehyde

Description:

(3,4-Diethoxyphenyl)(oxo)acetaldehyde, with the CAS number 952-17-0, is an organic compound characterized by its distinctive functional groups and structural features. It contains a phenyl ring substituted with two ethoxy groups at the 3 and 4 positions, which contribute to its hydrophobic character and influence its reactivity. The presence of the aldehyde functional group (-CHO) indicates that it can participate in various chemical reactions, such as nucleophilic addition and condensation reactions. This compound is likely to exhibit moderate solubility in organic solvents due to its non-polar ethoxy substituents, while its aldehyde group may impart some polarity. Additionally, the compound may display interesting biological activities, making it of interest in medicinal chemistry. Its synthesis typically involves the reaction of appropriate precursors under controlled conditions to ensure the desired substitution pattern on the phenyl ring. Overall, (3,4-diethoxyphenyl)(oxo)acetaldehyde is a versatile compound with potential applications in organic synthesis and pharmaceuticals.

Formula: C₁₂H₁₄O₄

InChI: InChI=1/C12H14O4/c1-3-15-11-6-5-9(10(14)8-13)7-12(11)16-4-2/h5-8H,3-4H2,1-2H3

InChI key: InChIKey=FQBWYMCPVZDSDB-UHFFFAOYSA-N

SMILES: O(CC)C1=C(OCC)C=CC(C(C=O)=O)=C1

Synonyms:

• Glyoxal, (3,4-diethoxyphenyl)-
• Benzeneacetaldehyde, 3,4-diethoxy-α-oxo-
• 3,4-Diethoxy-α-oxobenzeneacetaldehyde
• 2-(3,4-Diethoxyphenyl)-2-oxoacetaldehyde
• (3,4-diethoxyphenyl)(oxo)acetaldehyde hydrate(SALTDATA: FREE)
• (3,4-DIETHOXYPHENYL)(OXO)ACETALDEHYDE HYDRATE
• 3.4-Diethoxyphenylglyoxal