Product Introduction: (2-Isopropylphenyl)boronic Acid

Overview
(2-Isopropylphenyl)boronic acid, with CAS number 89787-12-2, is a versatile organic compound that plays a crucial role in synthetic chemistry and material science. Known alternatively as Boronic acid, B-[2-(1-methylethyl)phenyl]- and [2-(Propan-2-yl)phenyl]boronic acid, this compound is characterized by its unique chemical properties that make it indispensable in various applications.

Chemical Properties
(2-Isopropylphenyl)boronic acid features a boron atom bonded to a phenyl ring substituted with an isopropyl group. Its molecular formula is C12H17B O2, with a molecular weight of approximately 194.08 g/mol. The compound exhibits solubility in polar solvents, making it suitable for various chemical reactions. Its stability and reactivity allow it to participate in Suzuki coupling reactions, a vital tool for the formation of carbon-carbon bonds in organic synthesis.

Synthesis and Preparation
The synthesis of (2-Isopropylphenyl)boronic acid can be achieved through several efficient routes. One common method involves the reaction of isopropylphenyl lithium with boron trifluoride etherate, followed by hydrolysis. This route ensures high yield and purity, facilitating its subsequent applications in pharmaceuticals and agrochemicals.

For laboratory preparation, meticulous attention is granted to purity standards, ensuring that the final product adheres to guidelines meet rigorous analytical criteria, such as NMR and HPLC analyses.

Applications
(2-Isopropylphenyl)boronic acid finds its primary applications in:

1. Cross-Coupling Reactions : Utilized in Suzuki-Miyaura coupling reactions to synthesize complex organic molecules, this compound is invaluable in drug discovery and development. Its use enables chemists to construct diverse libraries of compounds efficiently.

2. Material Science : The compound plays a role in the development of polymeric materials and organic electronics. Its boronic acid functional group allows for the formation of dynamic covalent bonds, enhancing the properties of various materials.

3. Chemical Sensors : Leveraging its sensitivity to sugar molecules, (2-Isopropylphenyl)boronic acid is integrated into chemical sensors for glucose detection, aiding in diabetes management.

Quality Standards
At Ningbo Inno Pharmchem, we prioritize quality assurance and compliance with international standards. Our (2-Isopropylphenyl)boronic acid is manufactured under stringent conditions to ensure high purity and consistency. Each batch undergoes thorough analytical testing to meet industry specifications, ensuring that our customers receive a reliable product.

Conclusion
As a leading manufacturer and supplier of (2-Isopropylphenyl)boronic acid, Ningbo Inno Pharmchem is committed to providing high-quality chemicals that empower researchers and industries alike. Whether you are engaged in synthetic chemistry, material innovation, or sensor development, our (2-Isopropylphenyl)boronic acid is an essential compound that can enhance your projects and lead to successful outcomes. Explore the potential of this versatile boronic acid today!

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