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Usage

Uses

Used in Wood Preservation:
2,3-Dichloro-4-nitrophenol is used as a preservative agent for wood to protect it from decay, fungi, and insect infestation, thereby extending its lifespan and maintaining its structural integrity.
Used in Textile and Leather Industries:
In the textile and leather industries, 2,3-Dichloro-4-nitrophenol is used as an antimicrobial agent to prevent the growth of bacteria and fungi that can cause deterioration and spoilage of these materials.
Used in Pesticide and Herbicide Production:
2,3-Dichloro-4-nitrophenol is used as an active ingredient in the formulation of pesticides and herbicides to control and eliminate unwanted plants and insects in agricultural settings.
Used in Dye and Pharmaceutical Manufacturing:
This chemical compound is also utilized in the manufacturing of dyes, where it contributes to the coloration of various products, and in the production of pharmaceuticals, where it may be a component of certain medications.
Used in Chemical Compound Synthesis:
2,3-Dichloro-4-nitrophenol is employed as a synthetic intermediate in the creation of other chemical compounds, highlighting its versatility in the chemical industry.

Upstream product

• 576-24-9 2,3-dichlorophenol 
• 3209-22-1 1,2-Dichloro-3-nitrobenzene 
• 108-95-2 phenol 
• 207238-21-9 Carbonic acid 2,3-dichloro-phenyl ester ethyl ester 

Downstream Products

• 113730-47-5 4-benzoyl-6,7-dichloro-2,3-dihydrobenzofuran-2-carboxylic acid 
• 113730-44-2 6,7-dichloro-2-hydroxymethyl-2,3-dihydrobenzofuran-4-yl phenyl ketone 
• 113730-34-0 2-amino-3,4-dichloro-5-methoxybenzophenone 
• 113730-42-0 2-allyl-4,5-dichloro-3-hydroxybenzophenone 
• 113730-40-8 3,4-dichloro-5-allyloxybenzophenone 
• 113730-36-2 3,4-dichloro-5-methoxybenzophenone 
• 113730-43-1 1-(2-Allyl-4,5-dichloro-3-hydroxy-phenyl)-propan-1-one 
• 113730-38-4 3,4-dichloro-5-hydroxybenzophenone 
• 113730-37-3 1-(3,4-Dichloro-5-methoxy-phenyl)-propan-1-one 
• 113730-41-9 1-(3-Allyloxy-4,5-dichloro-phenyl)-propan-1-one 
• 113730-39-5 3',4'-dichloro-5'-hydroxypropiophenone 
• 113730-35-1 1-(2-Amino-3,4-dichloro-5-methoxy-phenyl)-propan-1-one 
• 105630-40-8 2,3-dichloro-4-methoxyaniline 
• 173456-54-7 1-(4-benzyloxy-2,3-dichlorophenyl)piperazine 

Relevant academic research and scientific papers

Hydroxylation of Nitroarenes with Alkyl Hydroperoxide Anions via Vicarious Nucleophilic Substitution of Hydrogen

Rhone-Poulenc Polska Ltd., ul. Grzybowska 80/82, 00-844 Warszawa, Poland Garbo- and heterocyclic nitroarenes react with anions of tert-butyl and cumyl hydroperoxides in the presence of strong bases to form substituted o- and p-nitrophenols. The reaction usually proceeds in high yields and is of practical value as a method of synthesis and manufacturing of nitrophenols. Orientation of the hydroxylation can be controlled to a substantial extent by selection of the proper conditions. Basic mechanistic features of this process were clarified.

Practical application of the palladium-catalyzed amination in phenylpiperazine synthesis: An efficient synthesis of a metabolite of the antipsychotic agent aripiprazole

A metabolite of Aripiprazole (1), 7-[4-[4-(2,3-dichloro-4- hydroxyphenyl)-1-piperaziyl]butoxy]-3,4-dihydro-2(1H)-quinolinone (2), was prepared by the coupling reaction of 1-(4-benzyloxy-2,3-dichlorophenyl) piperazine (11) with 7-(4-chlorobutoxy)-3,4-dihydro-2(1H)-quinolinone (16). The palladium-catalyzed amination of contiguous tri- and tetra-substituted benzenes with piperazine derivatives was investigated. The key intermediate 11 was efficiently prepared using the palladium-catalyzed amination of phenyl bromide 15 with piperazine.

6,7-dihalomelatonins

6,7-Dichloromelatonin and related compounds are ovulation inhibitors of the formula STR1 wherein R and R1 are individually F or Cl, R2 is C1-3 alkyl, including methyl, ethyl, n-propyl and isopropyl, and R3 is H or methyl.