Auxiliar de síntese eficiente: Ácido 4-Bromo-2,3,5,6-Tetrafluorofenilborónico para soluções de quimio-seletividade

2025-3-21

Efficient Synthesis Aid: 4-Bromo-2,3,5,6-Tetrafluorophenylboronic Acid for Chemo Selectivity Solutions

Chemical synthesis is a critical process in the pharmaceutical, agrochemical, and material science industries. The development of efficient and selective synthetic methods is essential for the production of high-quality compounds. In this guide, we will explore the use of 4-Bromo-2,3,5,6-tetrafluorophenylboronic acid as an efficient synthesis aid for achieving chemical selectivity in various reactions. This guide aims to provide a comprehensive overview of the product, its applications, and the benefits it offers to researchers and manufacturers.

Visão geral do produto

4-Bromo-2,3,5,6-tetrafluorophenylboronic acid is a highly selective boronic acid derivative that is widely used in chemical synthesis. It is characterized by its unique fluorinated and brominated substituents, which enhance its reactivity and selectivity in various reactions. The product is available in high purity and is suitable for use in both research and industrial applications.

Parâmetros do produto

Parâmetro	Valor
Aparência	Pó cristalino branco
Peso molecular	318.89 g/mol
Pureza	≥98%
Ponto de ebulição	≥300°C
Condição de armazenamento	Conservar em local fresco e seco, ao abrigo da luz e da humidade

Aplicações

4-Bromo-2,3,5,6-tetrafluorophenylboronic acid is a versatile reagent that finds applications in various chemical transformations. Some of the key applications include:

As a selective boronic acid derivative in Suzuki coupling reactions
For the synthesis of fluorinated compounds
In the preparation of biologically active molecules

Casos de utilização

Here are a few examples of how 4-Bromo-2,3,5,6-tetrafluorophenylboronic acid has been used in real-world applications:

Case 1: Suzuki Coupling Reaction

In a research study published in the Journal of Organic Chemistry, 4-Bromo-2,3,5,6-tetrafluorophenylboronic acid was used as a selective boronic acid derivative in a Suzuki coupling reaction. The study demonstrated the high efficiency and selectivity of the product in the synthesis of a complex fluoroaryl boronic acid derivative.

Case 2: Synthesis of Fluorinated Compounds

In another study, 4-Bromo-2,3,5,6-tetrafluorophenylboronic acid was employed in the synthesis of fluorinated compounds. The researchers successfully synthesized a series of fluoroaryl boronic acids using this reagent, which were further used in the development of novel agrochemicals.

Case 3: Preparation of Biologically Active Molecules

In a collaborative effort between a pharmaceutical company and a research institution, 4-Bromo-2,3,5,6-tetrafluorophenylboronic acid was used in the preparation of biologically active molecules. The product played a crucial role in the synthesis of a novel compound with potential therapeutic applications.

Soluções

4-Bromo-2,3,5,6-tetrafluorophenylboronic acid offers several advantages as an efficient synthesis aid:

High selectivity in various chemical transformations
Enhanced reactivity due to fluorinated and brominated substituents
Elevada pureza e estabilidade

Orientação especializada

For optimal results, it is recommended to follow the guidelines provided by the manufacturer. This includes proper handling, storage, and dosage of the product. Additionally, it is advisable to consult with an expert in the field for specific applications and reaction conditions.

Conclusão

4-Bromo-2,3,5,6-tetrafluorophenylboronic acid is a valuable tool for achieving chemical selectivity in various synthetic reactions. Its unique properties make it an efficient synthesis aid for the production of high-quality compounds in the pharmaceutical, agrochemical, and material science industries. By following the guidelines provided in this guide, researchers and manufacturers can maximize the benefits of this product in their chemical synthesis processes.

Palavras-chave

4-Bromo-2,3,5,6-tetrafluorophenylboronic acid, synthesis aid, chemical selectivity, Suzuki coupling, fluorinated compounds, biologically active molecules