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Structure of 1130146-98-3
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This piperidinol derivative features a 4-amino-3-ethoxyphenyl group linked to a hydroxylated piperidine scaffold, delivering a bench-stable, moisture-tolerant core for medicinal chemistry applications. The electron-rich aromatic moiety integrates readily into bioactive scaffolds, while the pendant hydroxyl enables strategic derivatization.
1-(4-Amino-3-ethoxyphenyl)piperidin-4-ol serves as a versatile building block for medicinal chemistry campaigns, enabling the construction of bioactive heterocycles through standard amide coupling and reductive amination protocols. The molecule combines a phenolic piperidinol core with an ethoxy-substituted aniline moiety, offering enhanced solubility and functional group tolerance. Its bench-stable nature facilitates straightforward purification and integration into multi-step syntheses of kinase inhibitors and CNS-targeted compounds.
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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-H312-H315-H319-H332-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: