5-Formyl-2-methoxybenzoic acid, with the CAS number 84923-70-6, is an organic compound that features a benzoic acid structure substituted with a formyl group and a methoxy group. This compound typically appears as a solid and is characterized by its aromatic nature, which contributes to its stability and reactivity. The presence of the formyl group (-CHO) indicates that it can participate in various chemical reactions, such as condensation and oxidation, making it a versatile intermediate in organic synthesis. The methoxy group (-OCH3) enhances its solubility in organic solvents and can influence its reactivity and interaction with other molecules. Additionally, the carboxylic acid functional group (-COOH) provides acidic properties, allowing for potential proton donation in chemical reactions. Overall, 5-formyl-2-methoxybenzoic acid is significant in synthetic organic chemistry, particularly in the development of pharmaceuticals and agrochemicals, due to its functional groups that enable diverse chemical transformations.

5-formyl-2-methoxybenzoic acid

84923-70-6: Benzoic acid, 5-formyl-2-methoxy-, 5-Formyl-2-methoxybenzoic acid

5-Formyl-2-methoxybenzoic acid

5-Formyl-2-methoxybenzoic acid is a hexamethylenetetramine that is used as an inhibitor of ATPase and proton pumps. It functions by binding to the active site of ATPase and blocking the release of ATP, which leads to decreased production of adenosine triphosphate (ATP). 5-Formyl-2-methoxybenzoic acid also inhibits the secretion of chloride ions from cells. 5-Formyl-2-methoxybenzoic acid has been found to inhibit glucose absorption in certain cells. This inhibition may be due to its ability to prevent insulin from binding with cells, leading to decreased levels of insulin and increased levels of glucagon.

CAS 84923-70-6: 5-formyl-2-methoxybenzoic acid

5-Formyl-2-methoxybenzoic acid

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5-Formyl-2-methoxybenzoic acid

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