792952-51-3

Usage

Uses

Used in Coordination Chemistry:
2-Chloro-4-hydroxy-5-nitrobenzoic acid is used as a chelating agent for metal complexation in coordination chemistry. Its ability to bind metal ions allows for the formation of stable complexes, which is useful in various chemical reactions and applications.
Used in Pharmaceutical Applications:
2-Chloro-4-hydroxy-5-nitrobenzoic acid is used as a potential pharmaceutical agent for its anti-inflammatory and neuroprotective properties. Its ability to modulate inflammatory pathways and protect neurons from damage makes it a promising candidate for the development of new drugs to treat inflammatory and neurodegenerative diseases.
Used in Metal Poisoning Treatment:
2-Chloro-4-hydroxy-5-nitrobenzoic acid is used as a potential treatment for metal poisoning due to its ability to chelate metal ions. By binding to toxic metal ions, it can help to reduce their harmful effects on the body and facilitate their removal from the system.

Upstream product

• 623-11-0 1-methyl-4-nitrosobenzene 
• 33458-98-9 2-chloro-4,5-dinitrobenzoic acid 
• 56363-84-9 2-chloro-4-hydroxybenzoic acid 
• 99-60-5 2-chloro-4-nitrobenzoic acid 
• 50-84-0 2,4 dichlorobenzoic acid 
• 118665-22-8 4-acetoxy-2-chloro-benzoic acid 
• 19861-62-2 2,4-dichloro-5-nitrobenzoic acid 

Downstream Products

• 190961-69-4 methyl 2-chloro-4-hydroxy-5-nitrobenzoate 
• 190961-70-7 methyl (R)-2-chloro-4-(2-octyloxy)-5-nitrobenzoate 
• 1428583-91-8 C₂₂H₁₄ClN₃O₆S 
• 1428583-87-2 ethyl 2-(4-(3-(benzo[d]thiazol-2-yl)phenylcarbamoyl)-5-chloro-2-nitrophenoxy)acetate 
• 1428583-84-9 C₂₁H₁₄ClN₃O₄S 
• 1428583-92-9 C₂₀H₁₂ClN₃O₄S 

Relevant academic research and scientific papers

Copper and L-(?)-quebrachitol catalyzed hydroxylation and amination of aryl halides under air

L-(?)-Quebrachitol, a natural product obtained from waste water of the rubber industry, was utilized as an efficient ligand for the copper-catalyzed hydroxylation and amination of aryl halides to selectively give phenols and aryl amines in water or 95percent ethanol. In addition, the hydroxylation of 2-chloro-4-hydroxybenzoic acid was validated on a 100-g scale under air.

Design of photonic liquid crystal materials: Synthesis and evaluation of new chiral thioindigo dopants designed to photomodulate the spontaneous polarization of ferroelectric liquid crystals

Irradiation of a ferroelectric S(c)* liquid crystal phase induced by the photochromic dopants (R,R)-6,6'-bis(2-octyloxy)-5,5'-dinitrothioindigo and (R,R)-5,5'-dichloro-6,6'-bis(2-octyloxy)thioindigo at λ=514 and 532 nm, respectively, causes an increase in spontaneous polarization (P(s)) by a factor ranging from 1.4 to 4.0. This increase in P(s) is achieved without concomitant destabilization of the S(c)* phase, and is consistent with an increase in transverse dipole moment of the thioindigo core as a result of trans-cis photoisomerization. The contribution of the thioindigo core towards P(s) is achieved through stereo-polar coupling with the chiral side-chains, which is enhanced by the presence of the nitro and chloro substituents.