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3-(DiMethylaMino)phenylboronic Acid Hydrochloride (contains varying aMounts of Anhydride) CAS:1256355-23-3

3-(Dimethylamino)phenylboronic acid hydrochloride is a boron-containing compound featuring a dimethylamino group attached to a phenyl ring at the meta position and a boronic acid functional group. The hydrochloride form enhances its solubility in water, making it suitable for various applications. This compound plays a crucial role in organic synthesis, particularly in medicinal chemistry, where it is used as a versatile building block for developing biologically active molecules. Its unique reactivity, especially in Suzuki-Miyaura cross-coupling reactions, enables the construction of complex organic structures important in pharmaceuticals and materials science.

 


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Application and Effect:

3-(Dimethylamino)phenylboronic acid hydrochloride is an essential compound in organic chemistry, serving multiple functions in both research and industrial applications. Its structure contains a boronic acid moiety that allows it to participate actively in cross-coupling reactions, especially Suzuki-Miyaura reactions, which are widely utilized in the synthesis of complex organic compounds. One of the primary applications of this compound is in the pharmaceutical industry. Its ability to form carbon-carbon bonds through cross-coupling reactions makes it a valuable intermediate in synthesizing a range of bioactive molecules, including potential drug candidates. Researchers have leveraged this compound to create derivatives with enhanced biological activity against various diseases, such as cancer and neurological disorders. The dimethylamino group can also influence the pharmacokinetics and binding properties of the resulting compounds, giving researchers further control over drug design. In addition to pharmaceuticals, 3-(dimethylamino)phenylboronic acid hydrochloride finds utility in agrochemicals. The versatility of the boronic acid functionality allows for the development of novel herbicides and pesticides. By modifying the phenyl ring or introducing additional substituents, chemists can tailor these compounds to target specific pests while aiming for minimal environmental impact. Furthermore, the compound is significant in materials science, particularly in the synthesis of functionalized polymers and nanomaterials. Its reactive boronic acid group can be used to create advanced materials with tailored properties for applications in electronics, sensors, and drug delivery systems. The presence of varying amounts of anhydride may affect its stability and reactivity, impacting how it is utilized in different chemical reactions. Understanding these variations is crucial for optimizing its performance in synthetic routes. In conclusion, 3-(dimethylamino)phenylboronic acid hydrochloride is a versatile compound with significant applications across pharmaceuticals, agrochemicals, and materials science. Its ongoing exploration continues to reveal new opportunities for innovation in chemical synthesis and application.

Product Sample:

L-Arginine1
L-Arginine2

Product Packing:

L-Arginin3

Additional Information:

Composition C8H13BClNO2
Assay 99%
Appearance white powder
CAS No.  1256355-23-3
Packing Small and bulk
Shelf Life 2 years
Storage Store in cool and dry area
Certification ISO.

 


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