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Understanding the Chemical Properties of 3-Bromopyridine (CAS 626-55-1)

For chemists and researchers involved in organic synthesis, a thorough understanding of the properties of chemical intermediates is fundamental. 3-Bromopyridine, a compound with the CAS number 626-55-1, is no exception. Its unique molecular structure and reactivity make it a cornerstone in the synthesis of a wide variety of complex molecules, particularly within the pharmaceutical and agrochemical sectors.

The molecular formula of 3-Bromopyridine is C5H4BrN. While the provided text does not explicitly detail its physical appearance beyond being a component in a list, it is generally known as a colorless to light yellow liquid. Key physical properties like its boiling point (around 172-174°C) and density (approximately 1.617 g/cm³) are critical for planning reactions, separations, and storage. These parameters, along with its purity, typically defined by standards like USP, BP, and FCC, are crucial when you buy 3-bromopyridine from a reputable supplier like NINGBO INNO PHARMCHEM CO.,LTD.

The significance of 3-bromopyridine chemical intermediate lies in its capacity to undergo various chemical transformations. The bromine atom attached to the pyridine ring is a good leaving group, making it amenable to nucleophilic substitution reactions, cross-coupling reactions (such as Suzuki, Heck, or Sonogashira couplings), and Grignard reagent formation. These reactions are vital for constructing carbon-carbon bonds and introducing new functional groups, thereby building complex molecular architectures required for pharmaceuticals and agrochemicals.

As NINGBO INNO PHARMCHEM CO.,LTD. continues to serve the chemical industry, understanding the detailed properties of compounds like 3-bromopyridine is key. Whether you are exploring new 3-pyridyl bromide applications or optimizing existing synthesis routes, having access to accurate chemical and physical data ensures efficient and successful outcomes in your research and development or manufacturing processes.

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