CAS 344287-58-7
:3-Benzofurancarboxylic acid, 7-methoxy-
Description:
3-Benzofurancarboxylic acid, 7-methoxy- is an organic compound characterized by its benzofuran structure, which consists of a fused benzene and furan ring. The presence of a carboxylic acid functional group (-COOH) at the 3-position and a methoxy group (-OCH3) at the 7-position contributes to its chemical reactivity and potential applications. This compound is likely to exhibit properties typical of carboxylic acids, such as acidity and the ability to form esters and amides. The methoxy group can influence the compound's solubility and polarity, making it more hydrophilic compared to its non-methoxylated counterparts. Additionally, the unique structural features may impart specific biological activities, making it of interest in medicinal chemistry and drug development. As with many organic compounds, its stability, reactivity, and interactions with other substances can vary based on environmental conditions such as pH and temperature. Overall, 3-Benzofurancarboxylic acid, 7-methoxy- represents a versatile structure with potential utility in various chemical and pharmaceutical applications.
Formula:C10H8O4
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Found 4 products.
7-methoxy-1-benzofuran-3-carboxylic acid
CAS:Formula:C10H8O4Purity:98%Color and Shape:SolidMolecular weight:192.16817-Methoxybenzofuran-3-carboxylic acid
CAS:7-Methoxybenzofuran-3-carboxylic acidPurity:98%Molecular weight:192.17g/mol7-Methoxy-1-benzofuran-3-carboxylic acid
CAS:<p>7-Methoxy-1-benzofuran-3-carboxylic acid is a precursor to thebaine and codeine. It is an ester with the chemical formula of CHONO2COOH, which can be synthesized by reacting 3,4-dimethoxybenzoic acid with diene. A regiospecific synthesis was developed for this compound in order to obtain the desired stereocontrolled product. The synthesis is done in two steps: cycloaddition followed by stereoselective intramolecular alkaloid formation.</p>Formula:C10H8O4Purity:Min. 95%Molecular weight:192.17 g/mol
