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2,3-Difluoro-4-ethoxybenzeneboronic acid CAS:212386-71-5

2,3-Difluoro-4-ethoxybenzeneboronic acid is a chemical compound classified as a boronic acid derivative. Its molecular structure comprises a boronic acid group attached to a benzene ring substituted with both difluoro and ethoxy functional groups. This compound holds significant importance in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a versatile boronic acid reagent. Additionally, its unique combination of electron-withdrawing and electron-donating substituents makes it valuable in medicinal chemistry, agrochemicals, and materials science.


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Application and Effect:

2,3-Difluoro-4-ethoxybenzeneboronic acid is a compound with distinct structural features and diverse applications in various fields of chemistry. 1. Synthetic Chemistry: Suzuki-Miyaura Cross-Coupling: This compound is widely utilized as a boronic acid reagent in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of biaryl compounds. Its versatile reactivity allows for the construction of complex molecules in organic synthesis, including pharmaceuticals, agrochemicals, and advanced materials. 2. Medicinal Chemistry: Drug Design: The difluoro and ethoxy substituents of 2,3-difluoro-4-ethoxybenzeneboronic acid impart unique properties that can influence drug-target interactions. This compound and its derivatives are explored in the design of pharmaceutical agents targeting various diseases, including cancer, inflammation, and infectious diseases. Fluorinated Pharmaceuticals: The presence of fluorine atoms in the molecule enhances the metabolic stability and pharmacokinetic properties of drugs, making fluorinated compounds valuable in medicinal chemistry for improving drug efficacy and selectivity. 3. Agrochemicals: Pesticide Development: Boronic acid derivatives, including 2,3-difluoro-4-ethoxybenzeneboronic acid, are utilized in the synthesis of agrochemicals such as herbicides, fungicides, and insecticides. Their structural diversity and reactivity allow for the design of compounds with improved efficacy and reduced environmental impact. Crop Protection: The development of boronic acid-based compounds contributes to crop protection strategies by providing novel solutions for controlling pests and diseases while minimizing risks to human health and the environment. 4. Materials Science: Functional Materials: 2,3-Difluoro-4-ethoxybenzeneboronic acid and its derivatives are incorporated into polymers and materials for various applications, including optoelectronics, sensors, and coatings. The unique properties of boronic acid-containing materials contribute to the development of functional materials with tailored properties and performance. In summary, 2,3-Difluoro-4-ethoxybenzeneboronic acid is a versatile compound with broad utility in synthetic chemistry, medicinal chemistry, agrochemicals, and materials science. Its distinctive structural features and reactivity offer opportunities for innovation and advancement in diverse areas of research and application.

Product Sample:

L-Arginine1
L-Arginine2

Product Packing:

L-Arginin3

Additional Information:

Composition C8H9BF2O3
Assay 99%
Appearance white powder
CAS No.  212386-71-5
Packing Small and bulk
Shelf Life 2 years
Storage Store in cool and dry area
Certification ISO.

 


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