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Structure of 100858-34-2
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(R)-Benzyl 3-hydroxypiperidine-1-carboxylate features a chiral piperidine core with a hydroxyl group at the 3-position, enabling stereoselective transformations in medicinal chemistry. The benzyl ester moiety provides stability and facilitates selective deprotection, streamlining access to functionalized piperidine scaffolds for drug discovery applications.
(R)-Benzyl 3-hydroxypiperidine-1-carboxylate serves as a stereochemically defined building block for the synthesis of bioactive piperidine derivatives. The hydroxyl group enables direct functionalization or protection, while the benzyl ester offers convenient deprotection under standard conditions. Its stability and compatibility with diverse reaction conditions facilitate integration into medicinal chemistry workflows, particularly for constructing chiral heterocyclic scaffolds in API development.
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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: