3798-89-8

Usage

Uses

Used in Pharmaceutical Industry:
1-Fluoro-3-phenoxybenzene is used as a key intermediate in the synthesis of various pharmaceutical compounds for its ability to be readily modified through chemical reactions. Its reactivity and stability contribute to the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, 1-Fluoro-3-phenoxybenzene is utilized as a precursor in the production of pesticides and other crop protection agents. Its chemical properties enable the creation of effective and targeted agrochemicals that can protect crops from pests and diseases.
Used in Polymer Production:
1-Fluoro-3-phenoxybenzene is used as a monomer or building block in the synthesis of polymers. Its incorporation into polymer chains can impart specific properties, such as enhanced stability or reactivity, which are desirable in various applications, including coatings, adhesives, and plastics.
Used in Specialty Chemicals:
As a versatile intermediate, 1-Fluoro-3-phenoxybenzene is also used in the production of specialty chemicals. Its unique properties allow it to be a component in the synthesis of dyes, fragrances, and other high-value chemical products that require specific characteristics for their intended uses.
Overall, 1-Fluoro-3-phenoxybenzene's diverse applications across different industries highlight its importance as a synthetic intermediate and building block in the chemical manufacturing sector. Its ability to undergo various chemical reactions and contribute to the development of new and improved products makes it a valuable compound in modern chemistry.

Upstream product

• 3586-12-7 3-phenoxyaniline 
• 108-95-2 phenol 
• 1073-06-9 3-fluorobromobenzene 
• 139-02-6 sodium phenoxide 

Downstream Products

• 105768-98-7 3-<4-(3-fluorophenoxy)benzoyl>acrylic acid 
• 101-84-8 diphenylether 
• 864772-18-9 4,4,5,5-tetramethyl-2-(3-phenoxyphenyl)-1,3,2-dioxaborolane 
• 23840-43-9 4′,6′-bis([1,1′-biphenyl]-4-yloxy)-5′-bromo-1,1′:3′,1″-terphenyl 
• 105769-02-6 2-acetylthio-3-<4-(3-fluorophenoxy)benzoyl>propionic acid 
• 105769-42-4 ethyl 3-<4-(3-fluorophenoxy)benzoyl>acrylate 

Relevant academic research and scientific papers

Trimethoxyphenyl (TMP) as a Useful Auxiliary for in situ Formation and Reaction of Aryl(TMP)iodonium Salts: Synthesis of Diaryl Ethers

Herein, we describe a synthetic approach for arylation that exploits the in situ formation and reaction of an unsymmetrical diaryliodonium salt. In this way, aryl iodides are used as reagents in a metal-free reaction with phenols, and a trimethoxyphenyl (TMP) group is used as a “dummy” group to facilitate transfer of a wide range of aryl moieties. The scope of aryl electrophiles and phenol nucleophiles is broad (>30 examples) and the yields are high (52–95%, 80% avg.). One-pot coupling reactions avoid the synthesis of diaryliodonium salts and provide opportunities for sequential reactions and novel chemoselectivity. (Figure presented.).

Hypervalent Iodine(III)-Catalyzed Balz–Schiemann Fluorination under Mild Conditions

An unprecedented hypervalent iodine(III) catalyzed Balz–Schiemann reaction is described. In the presence of a hypervalent iodine compound, the fluorination reaction proceeds under mild conditions (25–60 °C), and features a wide substrate scope and good functional-group compatibility.

Application of trivalent iodine compounds as catalysts in Bal-Schiemann reaction

The invention discloses an application of trivalent iodine compounds shown in formula I and/or II in the description and used as catalysts in Bal-Schiemann reaction. The trivalent iodine compounds areused as the catalysts in the Bal-Schiemann reaction, so that the Bal-Schiemann reaction can be conducted at room temperature or near room temperature when a thermochemical method is used, and the reaction has mild reaction conditions, wide substrate use range and short reaction time, and is safe and easy to operate, products are easy to separate, and raw materials are simple and low in toxicity.

POLYCYCLIC AROMATIC COMPOUND AND LIGHT EMISSION LAYER-FORMING COMPOSITION

The objective of the invention is to provide a polycyclic aromatic compound in which solubility to a solvent, film formability, wet coatability, thermal stability, and in-plane orientation are improved. This objective is achieved by a light emission layer

Polycyclic aromatic compound

The present invention addresses the problem of providing a novel polycyclic aromatic compound and an organic electroluminescent element using the same. The above problem is solved by providing a novel polycyclic aromatic compound in which a plurality of aromatic rings are connected by boron atoms, oxygen atoms, or the like, thereby increasing the number of options for organic EL element materials, and also solved by providing a superior organic EL element using said novel polycyclic aromatic compound as an organic EL element material.