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(3S,4R)-tert-Butyl 4-amino-3-fluoropiperidine-1-carboxylate

  • CAS No. 907544-20-1

  • Cat. No. CS-0058582
  • Purity≥97%
  • MDL No.MFCD17976872

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

(3S,4R)-tert-Butyl 4-amino-3-fluoropiperidine-1-carboxylate|CS-0058582

Structure of 907544-20-1

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General Information

  • CAS No. 907544-20-1
  • Cat. No. CS-0058582
  • Purity ≥97%
  • MDL No. MFCD17976872
  • Storage 4°C, protect from light
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₀H₁₉FN₂O₂
  • Molecular Weight 218.27
  • Synonym(s) tert-butyl (3S,4R)-4-aMino-3-fluoropiperidine-1-carboxylate
  • SMILES F[C@@H]1[C@H](N)CCN(C(OC(C)(C)C)=O)C1

Description

This chiral piperidine derivative features a tert-butyl carbamate-protected amine and a fluorine substituent at the 3-position, enabling selective incorporation into bioactive molecules. The (3S,4R) stereochemistry ensures precise spatial orientation for downstream applications in medicinal chemistry and peptide synthesis. Bench-stable and moisture-tolerant, it integrates seamlessly into complex molecule assembly workflows.

Application

(3S,4R)-tert-Butyl 4-amino-3-fluoropiperidine-1-carboxylate serves as a stereochemically defined building block for fluorinated piperidine scaffolds prevalent in medicinal chemistry. The protected amine and fluorinated C3 position enable selective functionalization, facilitating downstream derivatization via nucleophilic substitution or reductive amination. Bench-stable and readily purified by chromatography, it functions effectively in peptide coupling, transition-metal-catalyzed cross-coupling, and heterocycle construction 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-H319
Precautionary Statements : P264-P280-P302+P352-P305+P351+P338-P312-P337+P313-P363-P501

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Computational Chemistry Data

  • TPSA   55.56
  • LogP   1.2926
  • H_Acceptors   3
  • H_Donors   1
  • Rotatable_Bonds   0

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