The utility of any chemical intermediate is defined by its reactivity and the synthetic pathways it can enable. 2-Bromo-4,5-difluorobenzonitrile, a product offered by NINGBO INNO PHARMCHEM CO.,LTD., exemplifies a cornerstone molecule for diverse organic synthesis applications due to its inherent chemical characteristics.

With the CAS identifier 64695-82-5, this compound features a robust benzonitrile core adorned with two fluorine atoms and a bromine atom. The electron-withdrawing nature of the nitrile and fluorine groups significantly activates the aromatic ring, particularly influencing the reactivity of the carbon-bromine bond. This makes the bromine atom an excellent leaving group, readily participating in various metal-catalyzed cross-coupling reactions, such as Suzuki, Stille, and Heck couplings. These reactions are pivotal for forming new carbon-carbon bonds, allowing for the construction of complex molecular frameworks essential in pharmaceuticals, agrochemicals, and materials science.

Furthermore, the fluorine atoms themselves can be subjected to nucleophilic aromatic substitution (SNAr) reactions under specific conditions, although the bromine is generally more reactive. The nitrile group also offers additional synthetic handles, capable of undergoing reduction to an amine or hydrolysis to a carboxylic acid. NINGBO INNO PHARMCHEM CO.,LTD. ensures that this intermediate is supplied with an assay of u226598.0%, guaranteeing the reliability and efficiency of these chemical transformations. For researchers looking to buy 2-bromo-4,5-difluorobenzonitrile, the predictable reactivity profile is a significant advantage, streamlining experimental design and execution.

The versatility of 2-bromo-4,5-difluorobenzonitrile as an organic synthesis intermediate is undeniable. Its ability to participate in a wide range of reactions makes it an indispensable tool for chemists aiming to synthesize novel compounds. NINGBO INNO PHARMCHEM CO.,LTD. supports this endeavor by providing a consistently high-quality product, enabling the scientific community to push the boundaries of chemical innovation.