86309-06-0

Usage

Uses

Used in Pharmaceutical Synthesis:
2-(2,4-DICHLOROPHENOXY)BENZENECARBALDEHYDE is used as a key intermediate in the synthesis of pharmaceuticals, contributing to the development of new drugs due to its unique chemical structure and reactivity.
Used in Agrochemical Production:
In the agrochemical industry, 2-(2,4-DICHLOROPHENOXY)BENZENECARBALDEHYDE is utilized as an intermediate for the production of various agrochemicals, potentially aiding in the development of more effective and targeted pest control agents.
Used in Dye and Pigment Manufacturing:
2-(2,4-DICHLOROPHENOXY)BENZENECARBALDEHYDE is employed as an intermediate in the manufacturing of dyes and pigments, where its chemical properties allow for the creation of a wide range of colorants for different applications.
Used in Organic Compounds Synthesis:
2-(2,4-DICHLOROPHENOXY)BENZENECARBALDEHYDE serves as an intermediate in the synthesis of other organic compounds, broadening its utility across various chemical processes and industries.
Used in Herbicide Development:
2-(2,4-DICHLOROPHENOXY)BENZENECARBALDEHYDE has been studied for its potential as a herbicide for weed control, indicating its possible use in agricultural applications to manage unwanted plant growth.
It is crucial to handle 2-(2,4-DICHLOROPHENOXY)BENZENECARBALDEHYDE with care due to its potential hazards if ingested, inhaled, or comes into contact with the skin, emphasizing the need for proper safety measures during its use and manipulation.

InChI:InChI=1/C13H8Cl2O2/c14-10-5-6-13(11(15)7-10)17-12-4-2-1-3-9(12)8-16/h1-8H

Upstream product

• 3757-76-4 sodium 2,4-dichlorophenolate 
• 6630-33-7 ortho-bromobenzaldehyde 
• 33838-32-3 potassium 2-formylphenolate 
• 120-82-1 1,2,4-Trichlorobenzene 
• 446-52-6 2-Fluorobenzaldehyde 
• 120-83-2 2,4-dichlorophenol 
• 175136-80-8 2-(2,4-dichlorophenoxy)benzonitrile 

Downstream Products

• 86308-90-9 2-(2,4-dichlorophenoxy)cinnamic acid 
• 361212-70-6 1-[2-(2,4-dichlorophenoxy)phenyl]methanol 
• 1005763-18-7 C₁₅H₁₅Cl₂NO 
• 46795-43-1 (2-hydroxyphenyl)-(2,4-dichlorophenyl)methanone 
• 1393639-36-5 C₁₄H₁₂Cl₂N₂OS 
• 1393639-45-6 C₁₅H₁₂Cl₂O₃S 
• 866950-90-5 C₁₅H₁₃Cl₂NO₂S 
• 91821-40-8 2,4-dichloro-9H-xanthen-9-one 
• 86308-91-0 <2-(2,4-dichlorophenoxy)phenyl>acetohydroxamic acid 
• 86308-89-6 3-<2-(2,4-dichlorophenoxy)phenyl>propionic acid 
• 70458-41-2 <2-(2,4-dichlorophenoxy)phenyl>acetyl chloride 
• 86308-88-5 2-<2-(2,4-dichlorophenoxy)phenyl>ethanol 
• 478032-58-5 2,4-Dichloro-1-(2-chloromethyl-phenoxy)-benzene 
• 34645-84-6 fenclofenac 

Relevant academic research and scientific papers

Discovery of Pyrazine-Carboxamide-Diphenyl-Ethers as Novel Succinate Dehydrogenase Inhibitors via Fragment Recombination

The discovery of novel succinate dehydrogenase inhibitors (SDHIs) has attracted great attention worldwide. Herein, a fragment recombination strategy was proposed to design new SDHIs by understanding the ligand-receptor interaction mechanism of SDHIs. Thre

Wake-promoting agents: Search for next generation modafinil: Part IV

In search of a next generation molecule to the novel wake promoting agent modafinil, a series of diphenyl ether derived wakefulness enhancing agents (in rat) was developed. From this work, racemic compound 16 was separated into its chiral enantiomers to p

Rearrangement of 2-aryloxybenzaldehydes to 2-hydroxybenzophenones by rhodium-catalyzed cleavage of aryloxy C-O bonds

Lost in the shuffle: An unprecedented rearrangement of the title compounds proceeds by the simultaneous rhodium-catalyzed cleavage of aryloxy C-O and aldehyde C-H bonds (see scheme). The reaction tolerates the presence of various catalytically reactive substituents such as aryl halides, nitrile, and esters.

1-(2-Phenoxyphenyl)methanamines: SAR for dual serotonin/noradrenaline reuptake inhibition, metabolic stability and hERG affinity

A novel series of 1-(2-phenoxyphenyl)methanamines is disclosed, which possess selective dual 5-HT and NA reuptake pharmacology. Analogues with good human in vitro metabolic stability, hERG selectivity and passive membrane permeability were identified.

Imidazo heterocyclic compounds

A novel class of imidazo heterocyclic compounds, pharmaceutical compositions comprising them and use thereof in the treatment and/or prevention of diseases and disorders related to the histamine H3 receptor. More particularly, the compounds are useful for the treatment and/or prevention of diseases and disorders in which an interaction with the histamine H3 receptor is beneficial.

Substituted (2-Phenoxyphenyl)acetic Acids with Antiinflammatory Activity. 1

The synthesis and antiinflammatory activity of a series of substituted (2-phenoxyphenyl)acetic acids are described.Initial screening in the adjuvant arthritis test showed that halogen substitution in the phenoxy ring enhanced activity considerably.Ulcerogenic potential, as measured by the minimum ulcerogenic dose (MUD), was low in almost all the acids tested. acetic acid possessed the most favorable combination of potency with low toxicity, including ulcerogenicity, and this compound is now in therapeutic use.