19861-62-2

Usage

Uses

Used in Agricultural Industry:
2,4-Dichloro-5-nitrobenzoic acid is used as a herbicide for controlling the growth of unwanted plants. It is effective in inhibiting cell division in plants, leading to their death, which is crucial for maintaining the health and productivity of crops.
Used as a Plant Growth Regulator:
In addition to its herbicidal properties, 2,4-Dichloro-5-nitrobenzoic acid can also be used as a plant growth regulator. It can help control and manipulate the growth of plants, making it a valuable tool in agricultural practices for optimizing crop yields and quality.
It is important to handle 2,4-Dichloro-5-nitrobenzoic acid with care and follow proper safety precautions when using it due to its potential effects on plant growth and the environment.

InChI:InChI=1/C7H3Cl2NO4/c8-4-2-5(9)6(10(13)14)1-3(4)7(11)12/h1-2H,(H,11,12)

Upstream product

• 50-84-0 2,4 dichlorobenzoic acid 
• 7664-93-9 sulfuric acid 
• 13014-18-1 2,4-dichlorobenzotrichloride 
• 197368-69-7 sodium 2,4-dichloro-5-nitrobenzoate 
• 2234-16-4 1-(2,4-dichlorophenyl)ethan-1-one 
• 61671-51-0 1-(2,4-dichloro-5-nitro-phenyl)-ethanone 

Downstream Products

• 792952-51-3 2-chloro-4-hydroxy-5-nitrobenzoic acid 
• 100622-86-4 (5-Chlor-4-nitro-2-carboxy-phenyl)-(4-methoxy-phenyl)-amin 
• 855952-71-5 4-chloro-2-[(3,4-dimethoxyphenyl)amino]-5-nitrobenzoic acid 
• 101495-62-9 methyl 2,4-dichloro-5-nitrobenzoate 
• 713-28-0 2,4-dichloro-5-nitro benzoyl chloride 
• 234107-54-1 3-nitro-4-chloro-N-(3,5-dimethoxyphenyl)anthranilic acid 
• 5131-58-8 2,4-diaminonitrobenzene 
• 218773-26-3 2-[(4-carboxyphenyl)amino]-5-chloro-4-nitrobenzoic acid 
• 127625-17-6 ethyl ester of 1-cyclopropyl-6-nitro-4-oxo-7-chloro-1,4-dihydroquinoline-3-carboxylic acid 
• 161040-78-4 6-Amino-1-tert-butyl-4-oxo-7-pyrrolidin-1-yl-1,4-dihydro-quinoline-3-carboxylic acid ethyl ester 
• 148926-94-7 ethyl ester of 3-dimethylamino-2-(5-nitro-2,4-dichlorobenzoyl)acrylic acid 
• 148926-95-8 ethyl ester of 3-cyclopropylamino-2-(5-nitro-2,4-dichlorobenzoyl)acrylic acid 
• 161040-76-2 6-Amino-1-tert-butyl-7-(4-methyl-piperazin-1-yl)-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid ethyl ester 
• 161040-31-9 (Z)-3-tert-Butylamino-2-(2,4-dichloro-5-nitro-benzoyl)-acrylic acid ethyl ester 

Relevant academic research and scientific papers

Optimization of 2,4-diarylanilines as non-nucleoside HIV-1 reverse transcriptase inhibitors

The current optimization of 2,4-diarylaniline analogs (DAANs) on the central phenyl ring provided a series of new active DAAN derivatives 9a-9e, indicating an accessible modification approach that could improve anti-HIV potency against wild-type and resis

Design, synthesis, and preclinical evaluations of novel 4-substituted 1,5-diarylanilines as potent HIV-1 non-nucleoside reverse transcriptase inhibitor (NNRTI) drug candidates

Twenty-one new 4-substituted diarylaniline compounds (DAANs) (series 13, 14, and 15) were designed, synthesized, and evaluated against wildtype and drug resistant HIV-1 viral strains. As a result, approximately a dozen new DAANs showed high potency with l

QUINAZOLINONE COMPOUNDS

The present invention relates to quinazolinone compounds, processes for their preparation and their use as pharmaceutical agents for the treatment of Parkinson's disease (PD). The quinazolinone compounds are of general formula (I).

Synthesis and antimycobacterial activities of novel 6-nitroquinolone-3-carboxylic acids

Various 1-(substituted)-1,4-dihydro-6-nitro-4-oxo-7-(sub-secondary amino)-quinoline-3-carboxylic acids were synthesized from 2,4-dichlorobenzoic acid by six step synthesis. The compounds were evaluated for antimycobacterial in vitro and in vivo against My

Process for the production of nitro derivatives of aromatic compounds

Nitroderivates of aromatic compounds which are difficult to nitrate, can readily be obtained by nitration providing that the aromatic compound is treated with nitric acid or another nitrating agent in the presence of aliphatic or cycloaliphatic hydrocarbons monosubstituted or polysubstituted by halogen, the nitro group or an alkyl sulphonyl group, and the nitro derivative formed subsequently isolated.