5006-38-2

Usage

Uses

Used in Flavoring Industry:
2,4,5-Trifluoroanisole is used as a flavoring agent, capitalizing on its sweet, aromatic scent to enhance the taste and aroma of food products and beverages.
Used in Pharmaceutical Production:
In the pharmaceutical industry, 2,4,5-Trifluoroanisole serves as a key component in the manufacturing process of various medications, contributing to the development of new drugs and therapies.
Used in Agrochemical Production:
2,4,5-Trifluoroanisole is also utilized in the production of agrochemicals, where it may play a role in the formulation of pesticides, herbicides, or other agricultural products to improve their effectiveness and performance.
Used as an Intermediate in Organic Synthesis:
2,4,5-TRIFLUOROANISOLE is employed as an intermediate in organic synthesis reactions, facilitating the creation of more complex molecules and contributing to the advancement of organic chemistry and related fields.
Environmental Considerations:
Given its potential as an environmental contaminant, 2,4,5-Trifluoroanisole requires careful management and disposal to minimize its impact on ecosystems and human health. Proper safety precautions, including the use of personal protective equipment and adherence to regulatory guidelines, are essential when handling 2,4,5-TRIFLUOROANISOLE.

InChI:InChI=1/C7H5F3O/c1-11-7-3-5(9)4(8)2-6(7)10/h2-3H,1H3

Upstream product

• 327-54-8 1,2,4,5-Tetrafluorobenzene 
• 865-33-8 potassium methanolate 
• 124-41-4 sodium methylate 
• 2268-16-8 2,4,5-trifluorophenol 
• 77-78-1 dimethyl sulfate 

Relevant academic research and scientific papers

Fluorine analogs of dicamba and tricamba herbicides; Synthesis and their pesticidal activity

Fluorine analogs of the dicamba and tricamba herbicides were synthesized. Their herbicide activities were compared with the activities of the pattern herbicides dicamba and tricamba.

REACTION OF AROMATIC COMPOUNDS WITH NUCLEOPHILIC REAGENTS IN LIQUID AMMONIA IV.* THE NUCLEOPHILIC AND PROTOPHILIC ACTIVITY OF METHOXIDE AND HYDROXIDE IONS IN REACTIONS WITH POLYFLUORINATED AROMATIC COMPOUNDS

In the reaction of polyfluorinated derivatives of benzene with potassium methoxide in liquid ammonia a fluorine atom is substituted by a methoxy group.With potassium hydroxide reactions involving removal of a proton from a ring carbon atom take place preferentially.The possibility of polyfluoroarylation and methylation catalyzed by potassium hydroxide in polyfluorinated aromatic compounds, based on capture of the polyflurinated aryl anion by the electrophile, was demonstrated.

Mechanisms for Reactions of Halogenated Compounds. Part 3. Variation in Activating Influence of Halogen Substituents in Nucleophilic Aromatic Substitution

Rate constants are reported for reactions of polyhalogeno-pyridines and -benzenes with sodium methoxide in methanol.Relative activating effects of individual fluorine and chlorine atoms at positions ortho, meta, and para to the reaction site are determined and compared with orders determined from reactions involving ammonia in aqueous dioxan.The results are remarkably similar.Additional support is provided for earlier explanations of the activating effects of ortho-fluorine and -chlorine.Activation parameters, determined for reactions of polyhalogenepyridines with ammonia in aqueous dioxan, clearly demonstrate that differences in reactivity along the series arise mainly from changes in activation energy.