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Structure of 199174-24-8
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(S)-1-Boc-(3-Hydroxymethyl)pyrrolidine features a chiral pyrrolidine core with a hydroxymethyl group at the 3-position and a Boc-protected amine at the 1-position. This configuration enables direct incorporation into complex molecular architectures, particularly in medicinal chemistry and natural product synthesis. The protected amine ensures stability during multi-step transformations, while the pendant hydroxyl group provides a handle for selective derivatization. Its bench-stable nature supports reliable use under standard reaction conditions.
(S)-1-Boc-(3-Hydroxymethyl)pyrrolidine serves as a versatile chiral building block in medicinal chemistry, enabling the synthesis of pyrrolidine-based scaffolds with defined stereochemistry. The Boc-protected amine and primary alcohol functionalities offer orthogonal reactivity for sequential transformations. Its bench-stable nature and compatibility with standard coupling and reduction protocols facilitate efficient access to complex heterocyclic intermediates and API candidates.
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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: