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Structure of 1125551-75-8
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(S)-Piperidin-3-ylmethanol hydrochloride features a chiral piperidine core with a primary alcohol handle, offering enhanced solubility and stability under standard conditions. This bench-stable derivative integrates readily into asymmetric synthesis workflows, serving as a key scaffold for medicinal chemistry applications requiring stereocontrolled functionalization.
(S)-Piperidin-3-ylmethanol hydrochloride serves as a versatile chiral building block in medicinal chemistry, enabling efficient access to piperidine-containing scaffolds prevalent in bioactive molecules. Its bench-stable hydrochloride salt form enhances handling and solubility, while the primary alcohol functionality facilitates straightforward derivatization via esterification, etherification, or oxidation. The stereogenic center supports enantioselective synthesis, making it valuable for constructing targeted API intermediates with defined stereochemistry.
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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: