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Structure of 1893408-11-1
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(S)-Tert-butyl 3,3-difluoro-4-hydroxypiperidine-1-carboxylate features a stereochemically defined piperidine core with dual fluorine atoms at the 3-position and a hydroxyl group at C4. This configuration imparts enhanced metabolic stability and modulates polarity, enabling efficient incorporation into bioactive molecules. The tert-butyl ester serves as a robust protecting group for amine synthesis, compatible with standard deprotection protocols. This compound functions as a key building block in medicinal chemistry, particularly for CNS-targeted therapeutics and kinase inhibitors.
(S)-Tert-butyl 3,3-difluoro-4-hydroxypiperidine-1-carboxylate serves as a versatile chiral building block for the synthesis of fluorinated piperidine scaffolds prevalent in medicinal chemistry. The difluoro substitution at C3 enhances metabolic stability and modulates basicity, while the hydroxyl group enables facile derivatization via etherification, esterification, or oxidation. The tert-butyl carbamate protects the amine during multi-step synthesis, offering excellent bench stability and compatibility with standard coupling conditions. This compound functions effectively in transition-metal-catalyzed cross-couplings and reductive aminations, supporting efficient access to complex heterocyclic architectures.
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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 : H315-H319
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Precautionary Statements : P264-P280-P302+P352-P362+P364
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Lot numbers can be found on the outside label of a product: