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CAS 960289-56-9

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trans-3-dimethylamino-4-hydroxy-1-Boc-Pyrrolidine

Description:
Trans-3-dimethylamino-4-hydroxy-1-Boc-pyrrolidine is a chemical compound characterized by its pyrrolidine ring structure, which is a five-membered nitrogen-containing heterocycle. The "trans" configuration indicates the specific spatial arrangement of substituents around the ring, influencing its stereochemistry and reactivity. The presence of a dimethylamino group contributes to its basicity and potential for nucleophilic reactions, while the hydroxy group provides sites for hydrogen bonding and increases its polarity. The Boc (tert-butyloxycarbonyl) protecting group is commonly used in organic synthesis to temporarily mask the amine functionality, facilitating selective reactions. This compound is often utilized in medicinal chemistry and drug development due to its structural features that may enhance biological activity. Its properties, such as solubility and stability, can be influenced by the presence of the Boc group and the overall molecular structure. As with many organic compounds, careful handling and storage are essential to maintain its integrity and prevent degradation.
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