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Structure of 1174020-44-0
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This chiral piperidine derivative features a fluoro group at the 3-position and a hydroxyl moiety at the 4-position, stabilized by a tert-butyl carbamate protecting group. The stereochemistry at C3 and C4 imparts distinct conformational control, enabling selective incorporation into complex molecular architectures. Bench-stable and moisture-tolerant, it serves as a key building block for bioactive molecule synthesis.
(3S,4S)-tert-Butyl 3-fluoro-4-hydroxypiperidine-1-carboxylate serves as a stereochemically defined building block for fluorinated piperidine scaffolds. The tert-butoxycarbonyl (Boc) group enables convenient protection and orthogonal deprotection, while the C3-fluoro and C4-hydroxy functionalities provide distinct sites for derivatization. This compound exhibits bench stability and facilitates selective functionalization in medicinal chemistry campaigns targeting bioactive heterocycles.
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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: