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

  • CAS No. 1228185-45-2

  • Cat. No. CS-0048529
  • Molecule weight218.27
  • Purity≥97%
  • MDL No.MFCD26516106

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

tert-Butyl (3S,4S)-4-amino-3-fluoropiperidine-1-carboxylate|CS-0048529

Structure of 1228185-45-2

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General Information

  • CAS No. 1228185-45-2
  • Cat. No. CS-0048529
  • Purity ≥97%
  • MDL No. MFCD26516106
  • Storage 4°C, protect from light
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₀H₁₉FN₂O₂
  • Molecular Weight 218.27
  • Synonym(s) (3S,4S)-tert-Butyl 4-amino-3-fluoropiperidine-1-carboxylate
  • SMILES CC(C)(OC(N1CC[C@@H]([C@H](C1)F)N)=O)C

Description

tert-Butyl (3S,4S)-4-amino-3-fluoropiperidine-1-carboxylate delivers a stereochemically defined fluorinated piperidine scaffold with enhanced metabolic stability. The tert-butyl ester group enables straightforward deprotection under mild acidic conditions, while the amino and fluorine substituents provide strategic handle points for diversification in medicinal chemistry campaigns.

Application

tert-Butyl (3S,4S)-4-amino-3-fluoropiperidine-1-carboxylate serves as a stereochemically defined building block for the synthesis of fluorinated piperidine-containing pharmaceuticals. The protected amine and fluorinated C3 position enable direct functionalization in late-stage diversification, while the tert-butyl carbamate group offers excellent bench stability and facile deprotection under mild acidic conditions. Its well-defined stereochemistry facilitates reproducible access to bioactive scaffolds in medicinal chemistry campaigns.

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-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501

Quality Control

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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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