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Structure of 21156-84-3
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This piperidine derivative features a flexible ethan-1-ol tether linking a 1-methylpiperidin-4-yl group to a hydroxyl-bearing carbon. The primary alcohol enables straightforward derivatization, while the tertiary amine imparts solubility and basic character. Designed for modular synthesis in medicinal chemistry, this scaffold integrates readily into bioactive molecules requiring balanced polarity and metabolic stability under standard bench conditions.
2-(1-Methylpiperidin-4-yl)ethan-1-ol serves as a versatile building block in medicinal chemistry, enabling the construction of bioactive scaffolds through standard coupling and functionalization reactions. Its piperidine core offers favorable solubility and metabolic stability, while the primary alcohol facilitates derivatization via esterification, etherification, or oxidation to aldehyde. The molecule exhibits bench stability and compatibility with common reaction conditions, supporting efficient synthesis workflows in API development and target-oriented synthesis.
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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: