84575-26-8

Usage

General Description

2-Amino-p-anisic acid hydrochloride, also known as 4-Anisidine hydrochloride, is a chemical compound used in the synthesis of pharmaceuticals, dyes, and organic pigments. It is a derivative of anisic acid and contains a p-anisidine group, which makes it useful in the production of azo dyes. 2-AMINO-P-ANISIC ACID HYDROCHLORIDE is also used in the preparation of pharmaceuticals as it can be converted into various intermediates. Additionally, it has been found to have antimicrobial and anti-inflammatory properties and is under investigation for potential medicinal uses. 2-Amino-p-anisic acid hydrochloride is typically manufactured through chemical synthesis and is available for purchase from various chemical suppliers.

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

Upstream product

• 50868-75-2 5’-methoxy-2’-methylacetanilide 
• 1513883-14-1 4-methoxy-2-[(2-oxobutanoyl)amino]benzoic acid 
• 50868-72-9 5-methoxy-o-toluidine 
• 17484-36-5 4-Methyl-3-nitroanisole 

Downstream Products

• 35214-95-0 2,3-Dihydro-5-hydroxypyrrolo<2,1-b>chinazolin-9(1H)-on 

Relevant academic research and scientific papers

Oxidative ring opening of 3-hydroxyquinoline-2,4(1H,3H)-diones into N-(α-ketoacyl)anthranilic acids Dedicated to Professor Slovenko Polanc on his 65th birthday

N-(α-Ketoacyl)anthranilic acids were prepared by oxidative ring opening of 3-hydroxyquinoline-2,4(1H,3H)-diones by using paraperiodic acid (H5IO6) or sodium periodate (NaIO4). The optimisation of the reaction conditions is

SYNTHETIC ANALOGS OF Peganum ALKALOIDS. I. SYNTHESIS OF METHOXY- AND HYDROXY-SUBSTITUTED DEOXYVASICINONES AND DEOXYPEGANINES

6-Methoxy-, 7-methoxy-, and 8-methoxydeoxyvasicinones have been synthesized by the reaction of substituted (3-methoxy-, 4-methoxy-, and 5-methoxy-) anthranilic acids with α-pyrrolidone.The demethylation of these compounds has given the corresponding hydroxy-substituted analogs of deoxyvasicinone, and the reduction of the products obtained with zinc in hydrochloric acid has given the hydroxy- and methoxy- analogs of deoxypeganine. 8-Hydrooxydeoxypeganine dimethyl-, ethyl-, and butylcarbamates have been obtained by the carbamoylation of 8-hydroxydeoxypeganine.