57076-84-3

Usage

Uses

Used in Pharmaceutical Synthesis:
1-(4-chlorophenyl)-3-(2,4-dichlorophenyl)-2-propen-1-one is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique chemical structure allows for the creation of new compounds with potential therapeutic applications.
Used in Agrochemical Synthesis:
In the agrochemical industry, 1-(4-chlorophenyl)-3-(2,4-dichlorophenyl)-2-propen-1-one is utilized as a starting material for the development of new agrochemicals, such as pesticides and herbicides. Its chemical properties enable the production of compounds that can effectively control pests and protect crops.
Used in Organic Synthesis Research:
1-(4-CHLOROPHENYL)-3-(2,4-DICHLOROPHENYL)-2-PROPEN-1-ONE is also used in research settings for studying organic synthesis reactions, such as Michael additions and Friedel-Crafts acylations. Its potential as a reactive intermediate makes it a valuable tool for understanding and developing new synthetic pathways in organic chemistry.

InChI:InChI=1/C15H9Cl3O/c16-12-5-2-11(3-6-12)15(19)8-4-10-1-7-13(17)9-14(10)18/h1-9H

Upstream product

• 1122500-49-5 C₁₅H₉Br₂Cl₃O 
• 99-91-2 para-chloroacetophenone 
• 874-42-0 2,4-dichlorobenzaldeyhde 

Downstream Products

• 1122500-49-5 C₁₅H₉Br₂Cl₃O 
• 489447-65-6 1-(4-chlorophenyl)-2-(2,4-dichlorophenyl)ethane-1,2-dione 

Relevant academic research and scientific papers

Environmentally benign synthesis of substituted pyrazoles as potent antioxidant agents, characterization and docking studies

Oxidative stress is an important cause of neurogenerative diseases; treatment with a reliable antioxidant with no side effects is a potential tool?to overcome with such diseases. The aim of this study is to explore new and effective antioxidants and their

Isoxazoles-a biocompatible radical scavenging agents: Citrus juice mediated environmentally benign synthesis and characterization

This study demonstrates the efficient eco-friendly synthesis of a series of isoxazole derivatives 5a-h through (3+2) annulation of chalcones 3a-h and hydroxylamine (4) in citrus juice medium. The synthesized compounds were characterized by spectroscopic a

Environment Friendly Synthesis of N′-(1,3-Diphenylallylidene)-1-ethyl-7-methyl-4-oxo-1,4-dihydro-1,8-naphthyridine-3-carbohydrazides: Crystal Structure and Their Anti-oxidant Potential

An environment friendly synthesis of novel hybrid pharmacophores derived from synergism of nalidixic acid and 1,3-diphenylprop-2-en-1-ones is described. Percent yield and reaction times of microwave assisted reactions have been compared with the reactions

KF-melamine formaldehyde resin (KF-MFR) as a versatile and efficient heterogeneous reagent for aldol condensation of aldehydes and ketones under microwave irradiation

KF-Melamine formaldehyde resin (KF-MFR) was demonstrated to be a highly efficient heterogenious catalyst for cross-aldol condensation under microwave irradiation. In this synthesis, various aldehydes and ketones were condensed together in the presence of supported KF on melamine-formaldehyde resin to afford different chalcone derivatives in good to excellent yields. KF-MFR proved to have unique termal and chemical resistance and can be reused for many consecutive runs without remarkable loss in catalytic activity. Copyright

Analgesic and antimicrobial studies of some 2,4-dichloro-5-fluorophenyl containing arylidenetriazolothiadiazines

2,4-Dichloro-5-fluorophenyl containing 7-arylidenetriazolothiadiazines were obtained by the reaction of 4-amino-3-(2,4-dichloro-5-fluorophenyl)-5-mercapto- 1,2,4-triazole with 2,3-dibromo-1,3-diarylpropan-1-ones, and also by the reaction of 4-amino-3-(2,4