52106-89-5

Usage

Uses

Used in Organic Synthesis:
Sodium 4-chloro-2-nitrophenolate is utilized as a reagent in organic synthesis, particularly for the production of pharmaceuticals and fine chemicals. Its unique chemical properties allow it to participate in nucleophilic substitution reactions, facilitating the formation of desired products in the synthesis process.
Used in Chemical Manufacturing:
In the chemical manufacturing industry, sodium 4-chloro-2-nitrophenolate is employed in the production of dyes, pigments, and other chemical products. Its ability to form complexes with transition metals contributes to the development of a range of colorants and specialty chemicals.
Safety Considerations:
Due to its potential health and environmental hazards, sodium 4-chloro-2-nitrophenolate should be handled and disposed of with care, adhering to established safety regulations. This ensures the protection of both individuals and the environment from any adverse effects associated with this chemical compound.

InChI:InChI=1/C6H4ClNO3.Na/c7-4-1-2-6(9)5(3-4)8(10)11;/h1-3,9H;/q;+1/p-1

Upstream product

• 89-64-5 p-chloro-o-nitrophenol 

Downstream Products

• 5305-91-9 3,9-Bis-(4-chlor-2-nitro-phenoxy)-2,4,8,10-tetraoxa-3,9-diphospha-spiro<5,5>undecan-3,9-disulfid 
• 1019479-95-8 1-[2-(4-Chloro-2-nitro-phenoxy)-phenyl]-ethanone 
• 15793-48-3 5-chloro-2-ethoxy aniline 
• 29267-47-8 Methyl-(4-chloro-2-nitro-phenyl)-phosphat 
• 86308-39-6 [2-(4-Chloro-2-nitro-phenoxy)-phenyl]-acetic acid 
• 95-85-2 2-hydroxy-5-chloro-aniline 

Relevant academic research and scientific papers

Catalytic applications of β-cyclodextrin/palladium nanoparticle thin film obtained from oil/water interface in the reduction of toxic nitrophenol compounds and the degradation of azo dyes

A supramolecular catalyst of Pd/β-cyclodextrin thin film is synthesized via a facile and one-pot procedure at an oil-water interface. Macrocyclic oligosaccharides of cyclodextrins with glucose units have a wide range of applications due to their hydrophobic and chiral interior. Due to the ability of this supramolecular catalyst to form inclusion complexes with small organic molecules, the as-synthesized catalyst was applied for the reduction of toxic nitroaromatic compounds (p, o, m-nitrophenol and 4-Cl-2-nitrophenol) and the degradation of harmful azo dyes (methyl orange and bismarck brown) with considerable results. This investigation illustrates the change of the catalyst properties in the presence of molecular receptors attached to the catalyst surface.