| Chemical Name: | (S)-2-(Boc-amino)-5-hexynoic acid |
| CAS Number: | 208522-16-1 |
| Product Number: | AG00BHWX(AGN-PC-0WAL9A) |
| Synonyms: | |
| MDL No: | |
| Molecular Formula: | C11H17NO4 |
| Molecular Weight: | 227.2570 |
The (S)-2-(Boc-amino)-5-hexynoic Acid is a valuable tool in chemical synthesis for its versatile applications. This compound is utilized as a chiral building block in the preparation of various pharmaceuticals, agrochemicals, and advanced materials. Its stereochemistry, conferred by the (S)-configuration, enables precise control over the stereochemical outcome of reactions, making it particularly useful in asymmetric synthesis. Due to the presence of the Boc (tert-butoxycarbonyl) protecting group on the amino moiety, this compound offers enhanced stability and selectivity during synthetic transformations. This functionality facilitates the introduction of the amino acid motif into target molecules with high efficiency and purity. Moreover, the alkyne group in the molecule serves as a versatile handle for further functionalization through click chemistry reactions, allowing for the facile construction of complex structures. In summary, (S)-2-(Boc-amino)-5-hexynoic Acid plays a crucial role in modern chemical synthesis strategies, enabling the efficient and controlled assembly of intricate molecular architectures.
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