6961-49-5

Usage

Uses

Used in Pharmaceutical Industry:
2-[(2-chlorophenyl)amino]acetic acid is used as a building block for the synthesis of various drugs and pharmaceutical products. Its versatile structure enables the development of new compounds with enhanced therapeutic properties.
Used in Medical Research:
2-[(2-chlorophenyl)amino]acetic acid is studied for its potential use in the treatment of certain medical conditions, such as cardiovascular and neurological disorders. Its pharmacological profile suggests that it may offer benefits in managing inflammation and pain associated with these conditions.

Upstream product

• 28362-60-9 N-(2-chloro-phenyl)-glycine nitrile 
• 95-51-2 o-chloroaniline 
• 79-11-8 chloroacetic acid 
• 138608-88-5 N-(2-chloro-phenyl)-glycine amide 

Downstream Products

• 858252-17-2 N-acetyl-N-(2-chloro-phenyl)-glycine 
• 1610875-45-0 N-(4-bromo-3-methoxyphenyl)-2-(2-chlorophenylamino)acetamide 
• 1610874-94-6 2-(2-chlorophenylamino)-N-(3-methoxy-4-(1H-pyrazol-4-yl)phenyl)acetamide 
• 1007879-75-5 (R)-2-(dimethylamino)-2-(2-chlorophenyl)acetic acid 
• 1092065-32-1 C₂₅H₂₄Cl₃N₅O₂ 
• 932-32-1 N-methyl-2-chloroaniline 

Relevant academic research and scientific papers

Chiral cyanoamines and methods of preparation

Methods for preparing chiral non-racemic cyanoamines are provided. The methods are useful, e.g., for preparing chiral amino acids.

Synthesis and biological activity of some bistriazole derivatives

A series of bis-(4-amino-5-mercapto-triazol-3-yl)alkanes, their Schiff bases and bis-(1,2,4-triazolo[3,4-b]-1,3,4-thiadiazol-4-yl)alkanes have been synthesized. The newly synthesized compounds have been screened for their antibacterial properties. Compounds 5h and 9f exhibit greater degree of antibacterial activity than the standard, Furacin.

Process for producing optically active alpha-amino acid and optically active alpha-amino acid amine

The present invention provides a process for efficiently producing an optically active α-amino acid and an optically active α-amino acid amide. After contacting with cells or processed cells thereof having an ability to asymmetrically hydrolyse, a water solvent is substituted with at least one solvent selected from the group consisting of linear, branched, or cyclic alcohol having 3 or more carbon atoms and the optically active α-amino acid is preferentially precipitated from the alcohol solution. The addition of basic compounds, particularly potassium compounds to the alcohol solution containing the optically active α-amino acid amide, which is obtained after the separation of the optically active α-amino acid, enables the purification of the amide without the inclusion of amino acid into amino acid amide. Thus, the amide is subjected to the step of racemization and then recycled.