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CAS 224824-22-0

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(S)-4-(2-(tert-butoxycarbonylamino)-3-methoxy-3-oxopropyl)phenylboronic acid

Description:
(S)-4-(2-(tert-butoxycarbonylamino)-3-methoxy-3-oxopropyl)phenylboronic acid is a boronic acid derivative characterized by its unique structural features, including a phenyl ring, a boronic acid functional group, and a tert-butoxycarbonyl (Boc) protected amino group. This compound typically exhibits properties associated with boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The presence of the Boc group suggests that it can be used as a protecting group for amines, facilitating the selective functionalization of other reactive sites. Additionally, the methoxy and oxo groups contribute to its reactivity and solubility in organic solvents. The stereochemistry indicated by the (S) designation suggests that the compound has a specific three-dimensional arrangement, which can influence its biological activity and interactions. Overall, this compound is of interest in the development of pharmaceuticals and in the study of boron-containing compounds in organic chemistry.
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