In the intricate world of organic synthesis, the selection of appropriate building blocks is fundamental to achieving desired molecular structures. 3-Amino-4-iodopyridine (CAS 105752-11-2) emerges as a particularly valuable reagent due to its unique structural features and reactivity. As a specialized chemical building block, it offers chemists a strategic starting point for constructing complex organic molecules, especially those within the realm of pharmaceuticals and agrochemicals.

The presence of an iodine atom at the C-4 position of the pyridine ring makes 3-Amino-4-iodopyridine an excellent substrate for a variety of metal-catalyzed cross-coupling reactions. These include, but are not limited to, Suzuki-Miyaura couplings (with boronic acids), Sonogashira couplings (with terminal alkynes), and Buchwald-Hartwig aminations (with amines). These transformations are powerful tools for forging new carbon-carbon and carbon-heteroatom bonds, enabling the efficient assembly of intricate molecular frameworks. For researchers seeking to perform these reactions, finding a reliable supplier of 3-Amino-4-iodopyridine is key to consistent experimental outcomes.

Furthermore, the amino group at the C-3 position can also be functionalized or can influence the regioselectivity of subsequent reactions on the pyridine ring. This dual reactivity enhances its utility, allowing for sequential introduction of different chemical moieties. This makes it an attractive choice for those looking to buy C5H5IN2 for multi-step synthesis projects where precise control over functional group placement is critical.

The demand for such specialized intermediates is consistently high among research and development teams in pharmaceutical companies, universities, and contract research organizations. They often search for terms like “4-iodopyridin-3-ylamine manufacturer price” or “buy 3-Amino-4-iodopyridine in China” to identify cost-effective and dependable sources. By leveraging our expertise as a supplier of this heterocyclic compound, we aim to support these efforts by providing high-quality material with guaranteed purity and timely delivery.

The utility of 3-Amino-4-iodopyridine extends beyond its role in cross-coupling reactions. It is also an important intermediate in the synthesis of various biologically active molecules, including potential drug candidates. Its pyridine core, a common motif in pharmaceuticals, combined with the versatile iodine substituent, provides a robust platform for medicinal chemistry exploration. For any organic synthesis challenge that requires a functionalized pyridine scaffold, considering 3-Amino-4-iodopyridine is a strategic choice for efficient and innovative chemical design.