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Structure of 115909-91-6
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Benzyl 4-(2-hydroxyethyl)piperidine-1-carboxylate features a piperidine core functionalized with a hydroxyethyl side chain and a benzyl ester group, enabling selective derivatization. This scaffold offers enhanced solubility and stability under standard conditions, facilitating its use in medicinal chemistry campaigns targeting CNS disorders and kinase inhibition.
Benzyl 4-(2-hydroxyethyl)piperidine-1-carboxylate serves as a versatile synthetic intermediate for piperidine-based scaffolds. The pendant hydroxyl group enables facile derivatization via esterification, etherification, or oxidation to carboxylic acid, while the benzyl ester offers orthogonal protection and ease of removal under mild hydrogenolysis conditions. Its stability, compatibility with standard coupling reactions, and utility in building complex heterocyclic architectures make it a practical choice for medicinal chemistry and process development workflows.
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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-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: