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CAS 1095708-32-9

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2-(tert-Butoxycarbonylamino)pyridine-4-boronic acid pinacol ester

Description:
2-(tert-Butoxycarbonylamino)pyridine-4-boronic acid pinacol ester is a chemical compound characterized by its boronic acid functionality, which is significant in organic synthesis, particularly in Suzuki coupling reactions. This compound features a pyridine ring, which contributes to its aromatic properties and potential for coordination with metal catalysts. The tert-butoxycarbonyl (Boc) group serves as a protective group for amines, enhancing the compound's stability and reactivity under specific conditions. The pinacol ester moiety indicates the presence of a pinacol-derived structure, which can influence solubility and reactivity. This compound is typically used in medicinal chemistry and material science due to its ability to form covalent bonds with various substrates. Its unique structure allows for selective reactions, making it valuable in the development of pharmaceuticals and agrochemicals. Additionally, the presence of boron in its structure may impart unique electronic properties, making it a subject of interest in the field of organoboron chemistry. Overall, this compound exemplifies the intersection of organic synthesis and functional group manipulation in modern chemistry.
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