2-Formylbenzeneboronic Acid: A Versatile Reagent for Organic Synthesis
In the realm of organic chemistry, the utility of a reagent is often defined by its versatility and the efficiency with which it enables the construction of complex molecular frameworks. 2-Formylbenzeneboronic acid (CAS 40138-16-7) is a prime example of such a valuable compound. Its bifunctional nature, possessing both a reactive aldehyde group and a boronic acid moiety, makes it a highly sought-after intermediate for a broad spectrum of synthetic applications. This white crystalline powder, known for its consistent purity of ≥98.0%, is an indispensable tool for researchers engaged in drug discovery, materials science, and fine chemical synthesis.
The cornerstone of 2-Formylbenzeneboronic acid's utility lies in its participation in various palladium-catalyzed cross-coupling reactions. The boronic acid functionality is particularly adept at undergoing Suzuki-Miyaura coupling with aryl or vinyl halides, forming new carbon-carbon bonds with remarkable efficiency and regioselectivity. This reaction is fundamental in constructing biaryl systems and other complex aromatic compounds that are prevalent in many pharmaceutical agents and advanced materials. The presence of the ortho-formyl group provides an additional handle for further functionalization, allowing for subsequent transformations such as reductive amination, Wittig reactions, or condensation reactions, thereby expanding the molecular diversity achievable from a single starting material.
Beyond Suzuki couplings, this versatile reagent can also participate in other important synthetic protocols. For instance, the boronic acid group can engage in Chan-Lam couplings, enabling the formation of carbon-heteroatom bonds (C-N, C-O, C-S). The aldehyde group itself is a reactive site that can be readily converted into other functional groups, offering extensive opportunities for downstream modifications. For laboratories and chemical manufacturers, securing a reliable supply of high-quality 2-Formylbenzeneboronic acid is crucial. When looking to purchase this reagent, understanding its specifications, such as melting point (115-120°C) and density (1.24 g/cm³), and ensuring a consistent purity of ≥98.0% from your supplier is paramount for reproducible and successful synthetic outcomes. Investing in a trusted manufacturer ensures the integrity of your research.
The strategic importance of 2-Formylbenzeneboronic acid in modern organic synthesis cannot be overstated. Its ability to participate in a wide array of reactions makes it a flexible building block for creating novel chemical entities. Whether you are developing new pharmaceuticals, functional materials, or specialized agrochemicals, incorporating this boronic acid derivative into your synthetic strategy can unlock new possibilities and accelerate your research progress. For those seeking to buy this essential reagent, partnering with experienced suppliers who prioritize quality and offer competitive pricing is a key factor for success.
Perspectives & Insights
Logic Thinker AI
“In the realm of organic chemistry, the utility of a reagent is often defined by its versatility and the efficiency with which it enables the construction of complex molecular frameworks.”
Molecule Spark 2025
“2-Formylbenzeneboronic acid (CAS 40138-16-7) is a prime example of such a valuable compound.”
Alpha Pioneer 01
“Its bifunctional nature, possessing both a reactive aldehyde group and a boronic acid moiety, makes it a highly sought-after intermediate for a broad spectrum of synthetic applications.”