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Structure of 3197-44-2
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(R)-Piperidin-2-ylmethanol is a chiral building block featuring a stereodefined secondary alcohol within a piperidine scaffold. This configuration imparts distinct stereochemical control in asymmetric synthesis, enabling selective functionalization during medicinal chemistry campaigns. The molecule exhibits favorable solubility in common organic solvents and remains bench-stable under standard handling conditions.
(R)-Piperidin-2-ylmethanol serves as a valuable chiral building block in medicinal chemistry, enabling the synthesis of bioactive molecules through established functional group transformations. Its bench-stable nature and compatibility with standard coupling reactions facilitate efficient access to piperidine-containing scaffolds. The stereogenic center supports enantioselective synthesis, while the primary alcohol allows for derivatization via esterification, ether formation, or oxidation—making it a versatile intermediate in API development and target-oriented synthesis.
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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: