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Structure of 1623432-63-2
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This chiral amino alcohol hydrochloride features a cyclopropyl group that imparts conformational rigidity, enhancing stereochemical stability. The primary amine and hydroxyl functionalities enable efficient coupling in peptide synthesis and serve as key handles for derivatization. Bench-stable and moisture-tolerant, it simplifies handling in process development workflows.
(S)-2-Amino-2-cyclopropylethan-1-ol hydrochloride serves as a stereochemically defined building block for bioactive molecule synthesis, offering a rigid cyclopropyl moiety adjacent to a chiral amino alcohol functional group. Its hydrochloride salt enhances bench stability and facilitates purification, while the primary amine and hydroxyl groups enable diverse transformations including derivatization, coupling reactions, and incorporation into heterocyclic scaffolds relevant to medicinal chemistry.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P280-P302+P352
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Lot numbers can be found on the outside label of a product: