2-Methoxy-6-nitrobenzoic acid is an aromatic compound characterized by the presence of both a methoxy group and a nitro group on a benzoic acid framework. The methoxy group (-OCH₃) is an electron-donating substituent, while the nitro group (-NO₂) is an electron-withdrawing group, which can influence the compound's reactivity and properties. This compound typically appears as a solid at room temperature and is soluble in organic solvents, reflecting its aromatic nature. It is often used in organic synthesis and may serve as an intermediate in the production of pharmaceuticals or agrochemicals. The presence of the carboxylic acid functional group (-COOH) contributes to its acidic properties, allowing it to participate in various chemical reactions, such as esterification or amidation. Additionally, the compound's nitro group can undergo reduction reactions, making it versatile in synthetic applications. Safety data should be consulted for handling and storage, as with all chemical substances, to ensure proper precautions are taken.

2-Methoxy-6-nitrobenzoic acid

53967-73-0: 2-Nitro-6-methoxybenzoic acid, Benzoic acid, 2-methoxy-6-nitro-, o-Anisic acid, 6-nitro-, 2-Methoxy-6-nitrobenzoic acid, 2-Methoxy-6-nitrobenzoic Acid

2-Methoxy-6-nitrobenzoic acid is a perchloric acid derivative that is used as a catalyst for the hydrogenation of indoles and indolines to their corresponding cinnolines. The substituent in 2-Methoxy-6-nitrobenzoic acid is methyl group. This compound can be isolated by recrystallization from water and has been shown to catalyze the hydrogenation of indole derivatives with palladium as a catalyst.

CAS 53967-73-0: 2-Methoxy-6-nitrobenzoic acid

2-Methoxy-6-nitrobenzoic acid

Ref: 10-F044372

2-Methoxy-6-nitrobenzoic acid

Ref: IN-DA003HJN

2-Methoxy-6-nitrobenzoic acid

Ref: 3D-DCA96773

2-Methoxy-6-nitrobenzoic acid

Ref: 54-OR90816