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Structure of 68327-11-7
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This chiral amino alcohol delivers a stereochemically defined scaffold for asymmetric synthesis, featuring a bench-stable hydrochloride salt form and a rigid cyclopentane ring that enforces conformational control. The primary amine and adjacent hydroxyl group enable direct functionalization in catalytic transformations and ligand development.
(1R,2R)-2-Aminocyclopentanol hydrochloride serves as a stereochemically defined chiral building block for the synthesis of bioactive heterocycles and medicinal intermediates. Its bench-stable hydrochloride salt form enables straightforward handling and purification, while the adjacent amine and alcohol functionalities offer orthogonal reactivity for derivatization in multistep sequences. This compound facilitates efficient access to cyclopentane-based scaffolds commonly found in pharmaceuticals and agrochemicals.
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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-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: