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Structure of 195202-09-6
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This chiral piperidine derivative features a sterically defined (S)-configured butanoyl side chain bearing a 3,4,5-trimethoxyphenyl group, enabling selective interactions in asymmetric synthesis. The carboxylic acid moiety provides a handle for coupling reactions, while the trimethoxy substitution enhances solubility and modulates electronic properties. Designed for use in medicinal chemistry campaigns targeting CNS-relevant scaffolds, this compound delivers structural complexity with predictable stereochemical integrity under standard bench conditions.
(S)-1-((S)-2-(3,4,5-Trimethoxyphenyl)butanoyl)piperidine-2-carboxylic acid serves as a versatile chiral building block for medicinal chemistry campaigns, enabling the synthesis of complex heterocyclic scaffolds. Its pendant 3,4,5-trimethoxyphenyl group enhances solubility and provides a robust handle for derivatization. The molecule exhibits excellent bench stability, facilitates straightforward purification via standard chromatography, and functions reliably in amide coupling and cyclization protocols common to API 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 : H302-H315-H319-H335
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Precautionary Statements : P261-P280-P302+P352
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Lot numbers can be found on the outside label of a product: