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CAS 145106-43-0

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(1S,2S)-trans-N-Boc-2-aminocyclopentanol

Description:
(1S,2S)-trans-N-Boc-2-aminocyclopentanol is a chiral compound characterized by its bicyclic structure, which includes a cyclopentane ring and an amino group. The "N-Boc" designation indicates that the amino group is protected by a tert-butyloxycarbonyl (Boc) group, a common protecting group in organic synthesis that enhances the stability and reactivity of the amine. The (1S,2S) configuration signifies the specific stereochemistry at the chiral centers, which is crucial for its biological activity and interactions. This compound is typically used in the synthesis of pharmaceuticals and other biologically active molecules due to its ability to serve as a building block in asymmetric synthesis. Its solubility and reactivity can vary depending on the solvent and conditions used, making it a versatile intermediate in organic chemistry. Additionally, the presence of the Boc group allows for selective deprotection, facilitating further functionalization of the amino group in subsequent reactions.
Formula:C10H19NO3
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