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    Home > Active Ingredient News > Active Ingredient Products News > The Instruction of B-[3-[(Butylamino)sulfonyl]phenyl]boronic acid

    The Instruction of B-[3-[(Butylamino)sulfonyl]phenyl]boronic acid

    • Last Update: 2023-05-08
    • Source: Internet
    • Author: User
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    Title: The Production of B-[3-[(Butylamino)sulfonyl]phenyl]boronic Acid: A Comprehensive Overview of its Synthesis, Applications, and Industrial Relevance


    Abstract:
    B-[3-[(Butylamino)sulfonyl]phenyl]boronic acid is an important organoboronic acid that has gained significant attention in recent years due to its diverse applications in various fields, including pharmaceuticals, agrochemicals, and materials science.
    This article provides a comprehensive overview of the synthesis of B-[3-[(Butylamino)sulfonyl]phenyl]boronic acid, its structures, and properties, as well as its industrial production, applications, and future trends.
    The article is divided into various sections, including a general introduction, the synthesis and properties of B-[3-[(Butylamino)sulfonyl]phenyl]boronic acid, its applications and industrial relevance, and concludes with a discussion on future prospects and challenges in the field.


    Introduction:
    Boric acid and its derivatives, including boronic acids, are widely used in various industrial applications.
    Boronic acids have unique properties, such as high acidity, Lewis acidity, and the ability to coordinate with metal ions, which make them ideal candidates for the synthesis of various materials and compounds.
    B-[3-[(Butylamino)sulfonyl]phenyl]boronic acid is an important organoboronic acid that has gained significant attention in recent years due to its diverse applications.
    This section provides an overview of the production of B-[3-[(Butylamino)sulfonyl]phenyl]boronic acid and its industrial relevance.


    Synthesis and Properties:
    B-[3-[(Butylamino)sulfonyl]phenyl]boronic acid can be synthesized using various methods, including chemical reduction, hydrolysis, and electrophilic substitution reactions.
    The most commonly used method is the reduction of B-[3-Chloro-2-oxo-1,2-oxazolidin-3-yl]boronic acid using various reducing agents, such as lithium aluminum hydride, hydrogen over palladium on barium oxide, and sodium borohydride.
    The structure and properties of B-[3-[(Butylamino)sulfonyl]phenyl]boronic acid have been studied extensively and it has been shown to have high water solubility, good thermal stability, and excellent catalytic properties.
    The chemical structure of B-[3-[(Butylamino)sulfonyl]phenyl]boronic acid is shown below:


    [B(C6H13NO2)2B(C4H9O3S2)][B(C6H5)2]


    Applications and Industrial Relevance:
    B-[3-[(Butylamino)sulfonyl]phenyl]boronic acid has diverse applications in various fields, including pharmaceuticals, agrochemicals, and materials science.
    In the field of pharmaceuticals, B-[3-[(Butylamino)sulfonyl]phenyl]boronic acid has been used as a catalyst for the asymmetric hydrogenation of various compounds, including aldehydes, ketones, and nitro compounds.
    In the field of agrochemicals, B-[3-[(Butylamino)sulfonyl]phenyl]boronic acid has been used as a catalyst for the synthesis of various pesticides, herbicides, and fungicides.
    In the field of materials science, B-[3-[(Butylamino)sulfonyl]phenyl]boronic acid has been used as a catalyst for the polymerization of various monomers and the synthesis of various polymers.
    It has also been used as


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