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(S)-1-((S)-2-(3,4,5-Trimethoxyphenyl)butanoyl)piperidine-2-carboxylic acid

  • CAS No. 195202-09-6

  • Cat. No. CS-0133828
  • Molecule weight365.43
  • Purity≥98%
  • MDL No.MFCD23698714

*For research and further manufacturing use only, not for direct human use.

(S)-1-((S)-2-(3,4,5-Trimethoxyphenyl)butanoyl)piperidine-2-carboxylic acid|CS-0133828

Structure of 195202-09-6

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General Information

  • CAS No. 195202-09-6
  • Cat. No. CS-0133828
  • Purity ≥98%
  • MDL No. MFCD23698714
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₉H₂₇NO₆
  • Molecular Weight 365.43
  • Synonym(s) None
  • SMILES O=C([C@H]1N(C([C@H](C2=CC(OC)=C(OC)C(OC)=C2)CC)=O)CCCC1)O

Description

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.

Application

(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.

Safety Information

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GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H302-H315-H319-H335
Precautionary Statements : P261-P280-P302+P352

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Computational Chemistry Data

  • TPSA   85.3
  • LogP   2.6717
  • H_Acceptors   5
  • H_Donors   1
  • Rotatable_Bonds   7

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