CAS 80893-99-8

Benzoic acid, 4-formyl-3-methoxy-

Description:

Benzoic acid, 4-formyl-3-methoxy- (CAS 80893-99-8) is an aromatic carboxylic acid characterized by the presence of a benzoic acid moiety with a formyl group and a methoxy group at specific positions on the benzene ring. This compound typically exhibits a white to off-white crystalline appearance and is soluble in organic solvents while having limited solubility in water due to its hydrophobic aromatic structure. The presence of the formyl group (-CHO) contributes to its reactivity, allowing it to participate in various chemical reactions, such as oxidation and condensation. The methoxy group (-OCH3) can influence the compound's electronic properties and steric hindrance, affecting its reactivity and interactions with other molecules. Benzoic acid derivatives are often studied for their potential applications in pharmaceuticals, agrochemicals, and as intermediates in organic synthesis. Additionally, the compound may exhibit biological activity, making it of interest in medicinal chemistry and related fields.

Formula: C₉H₈O₄

4-Formyl-3-methoxybenzoic acid

CAS: 80893-99-8

Formula: C₉H₈O₄

Purity: 95%

Color and Shape: Solid

Molecular weight: 180.1574

Ref: IN-DA0039ZA

4-Formyl-3-methoxybenzoic acid

CAS: 80893-99-8

4-Formyl-3-methoxybenzoic acid

Purity: 97%

Molecular weight: 180.16g/mol

Ref: 54-OR1005606

4-FORMYL-3-METHOXYBENZOIC ACID

CAS: 80893-99-8

Formula: C₉H₈O₄

Purity: 97%

Molecular weight: 180.159

Ref: 10-F513953

4-Formyl-3-methoxybenzoic acid

CAS: 80893-99-8

4-Formyl-3-methoxybenzoic acid is a sulfamic acid derivative that has been used in the treatment of asthma. It is a prodrug that converts to its active form, methanesulfonic acid, by enzymatic transfer. The target product of this reaction is zafirlukast, which competitively blocks leukotrienes at the cysteinyl leukotriene receptor. Methanesulfonic acid acts as an inhibitor of hydrogen transfer and may also act as a proton ionophore in the lungs. 4-Formyl-3-methoxybenzoic acid can be synthesized on a large scale with chemical products that are readily available. This agent reacts with proline and protonates it.

Formula: C₉H₈O₄

Purity: Min. 95%

Molecular weight: 180.16 g/mol

Ref: 3D-FDA89399