Suzuki-Miyaura Coupling: The Role of 3-Chloro-4-carboxyphenylboronic Acid
The Suzuki-Miyaura cross-coupling reaction is a cornerstone of modern organic synthesis, celebrated for its efficiency and versatility in forming carbon-carbon bonds. This palladium-catalyzed reaction has revolutionized the synthesis of complex molecules, particularly in the pharmaceutical and agrochemical industries. At the heart of this reaction are organoboron compounds, with boronic acids being among the most widely used. Understanding the specific utility of different boronic acid derivatives is crucial for chemists aiming to optimize their synthetic routes.
One such highly functionalized boronic acid is 3-Chloro-4-carboxyphenylboronic acid, also known by its CAS number 136496-72-5. This molecule is a prime example of how carefully designed intermediates can unlock new synthetic possibilities. The presence of both a carboxylic acid group and a chlorine atom on the phenyl ring offers multiple avenues for further chemical transformations. The carboxylic acid moiety can serve as a point for amide or ester formation, or it can influence solubility and biological interactions. The chlorine atom can participate in further cross-coupling reactions or act as an electronic modulating substituent.
When chemists and procurement specialists look to buy this specific boronic acid derivative, they often seek it for its crucial role in synthesizing complex APIs or novel agrochemical compounds. The Suzuki-Miyaura coupling provides a robust method to attach this substituted phenyl group to various organic halides or triflates, thereby building molecular complexity efficiently. As a reputable manufacturer and supplier in China, we provide 3-Chloro-4-carboxyphenylboronic acid with a high guaranteed purity, essential for the success of these demanding reactions. Competitive price and consistent quality are hallmarks of our service.
The utility of 3-Chloro-4-carboxyphenylboronic acid is well-documented in scientific literature for its application in medicinal chemistry and materials science. Its specific structural features allow for the precise construction of target molecules, leading to compounds with tailored properties. For anyone involved in research and development, ensuring a reliable source for such key intermediates is vital. By partnering with an experienced chemical producer, you can streamline your procurement process and focus on innovation.
If your research or production involves Suzuki-Miyaura coupling or requires a versatile functionalized phenylboronic acid, consider exploring the offerings from trusted chemical suppliers. We are dedicated to supporting your projects with high-quality intermediates, ensuring that your synthetic endeavors are both efficient and successful. Reach out to us to learn more about our products and how we can meet your chemical needs.
Perspectives & Insights
Silicon Analyst 88
“When chemists and procurement specialists look to buy this specific boronic acid derivative, they often seek it for its crucial role in synthesizing complex APIs or novel agrochemical compounds.”
Quantum Seeker Pro
“The Suzuki-Miyaura coupling provides a robust method to attach this substituted phenyl group to various organic halides or triflates, thereby building molecular complexity efficiently.”
Bio Reader 7
“As a reputable manufacturer and supplier in China, we provide 3-Chloro-4-carboxyphenylboronic acid with a high guaranteed purity, essential for the success of these demanding reactions.”