2840-26-8

Usage

Uses

Used in Organic Synthesis:
3-Amino-4-methoxybenzoic acid is used as a key intermediate for the synthesis of various organic compounds, contributing to the development of new materials and products in the chemical industry.
Used in Pharmaceutical Applications:
3-Amino-4-methoxybenzoic acid is used as a general reactant/reagent for the synthesis of VEGFR-2 inhibitors, which are important in the treatment of certain types of cancer by inhibiting angiogenesis, the process through which new blood vessels form.
Used in the Preparation of Dihydroisoquinoline Compounds:
In the pharmaceutical industry, 3-Amino-4-methoxybenzoic acid is also utilized in the preparation of dihydroisoquinoline compounds, which act as tubulin polymerization inhibitors. These compounds have potential applications in cancer therapy by disrupting the normal cell division process in cancer cells.
Used in Agrochemicals:
3-Amino-4-methoxybenzoic acid is employed as a vital raw material in the agrochemical sector, where it is used to develop compounds that can protect crops from pests and diseases, ensuring increased agricultural productivity.
Used in Dyestuffs:
In the dyestuffs industry, 3-Amino-4-methoxybenzoic acid is used as an essential intermediate for the production of various dyes and pigments, contributing to the vibrant colors and hues in textiles, plastics, and other materials.

InChI:InChI=1/C8H9NO3/c1-12-7-3-2-5(8(10)11)4-6(7)9/h2-4H,9H2,1H3,(H,10,11)/p-1

Upstream product

• 89-41-8 4-methoxy-3-nitrobenzoic acid 
• 24812-90-6 methyl 3-amino-4-methoxybenzoate 
• 7647-01-0 hydrogenchloride 
• 10034-85-2 hydrogen iodide 
• 40757-20-8 methyl 4-methoxy-3-nitrobenzoate 
• 99-58-1 3-bromo-4-methoxybenzoic acid 
• 954815-08-8 3-bromo-4-methoxy-5-nitro-benzoic acid 
• 110-53-2 1-Bromopentane 

Downstream Products

• 66832-25-5 3-((Z)-3-Carboxy-acryloylamino)-4-methoxy-benzoic acid 
• 120623-41-8 7-(3-amino-4-methoxyphenyl)-N-(2-hydroxy-5-oxocyclopent-1-enyl)hepta-2,4,6-trienamide 
• 90-04-0 2-methoxy-phenylamine 
• 15719-64-9 methylammonium carbonate 
• 306937-12-2 3-[(tert-butyloxycarbonyl)amino]-4-methoxybenzoic acid 
• 434315-19-2 Ph₂PCH₂NHC₆H₃(3-COOH)(6-OCH₃) 
• 256935-69-0 N-Fmoc 3-amino-4-methoxy-benzoic acid 
• 148887-46-1 quinoline-8-methoxy-5-carboxylic acid 
• 24812-90-6 methyl 3-amino-4-methoxybenzoate 
• 709044-26-8 butyl 3-(4-methyl-1-piperazinyl)-4-methoxybenzoate 
• 1000068-59-6 3-[(6-chloropyrazin-2-yl)amino]-4-methoxybenzoic acid 

Relevant academic research and scientific papers

Microwave thermolysis VII: Selective diversity in the reduction using sodium hypophosphite under microwave irradiation

The selective reduction of nitro group into amine using sodium hypophosphite under microwave irradiation is described. The rapid reaction, solvent free conditions and selectivity over common functional groups like CN, OH, COOH, CONH2 and halogens are the distinct features of the procedure.

Compounds and pharmaceutical use thereof

PCT No. PCT/JP97/00291 Sec. 371 Date Aug. 6, 1998 Sec. 102(e) Date Aug. 6, 1998 PCT Filed Feb. 6, 1997 PCT Pub. No. WO97/29079 PCT Pub. Date Aug. 14, 1997The compounds of the formula (I) wherein each symbol is as defined in the specification, pharmaceutically acceptable salts thereof and pharmaceutical use thereof. The Compound (I) and pharmaceutically acceptable salts thereof of the present invention selectively act on cannabinoid receptors, particularly peripheral receptors, cause less side effects on the central system, and have superior immunoregulating action, antiinflammatory action, antiallergic action and therapeutic effect on nephritis. Therefore, they are useful as cannabinoid receptor, particularly peripheral cannabinoid receptor activators and antagonists, immunoregulators, therapeutic agents for autoimmune diseases, antiinflammatory agents, antiallergic agents and therapeutic agents for nephritis.

A GENERAL PROCEDURE FOR MILD AND RAPID REDUCTION OF ALIPHATIC AND AROMATIC NITRO COMPOUNDS USING AMMONIUM FORMATE AS A CATALYTIC HYDROGEN TRANSFER AGENT

Various aliphatic and aromatic nitro compounds were selectively and rapidly reduced to their corresponding amino derivatives in very good yield using anhydrous ammonium formate as a catalytic hydrogen transfer agent.

One step diazotization coupling process

A process for producing metal-free azo pigments in purely organic liquid or aqueous/organic liquid containing at most 10% of water calculated on the total weight of the suspension is described. In this one-step process, a suitable aromatic amine is diazotized without isolation of the obtained diazo compound and coupled with a coupling component. Both reactions are carried out in purely or essentially organic medium. The latter consists essentially of such amount of an organic liquid that a substantial portion either of the diazo component or of the coupling component or of both these reactants remain undissolved. Both reactants must be free from sulphonic acid groups. If the resulting azo pigment contains carboxylic acid groups, these can be subsequently converted to the corresponding amido or ester groups.