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

  • CAS No. 1260612-08-5

  • Cat. No. CS-0058589
  • Purity≥98%
  • MDL No.MFCD12756122

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

(3R,4R)-tert-Butyl 4-amino-3-fluoropiperidine-1-carboxylate|CS-0058589

Structure of 1260612-08-5

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General Information

  • CAS No. 1260612-08-5
  • Cat. No. CS-0058589
  • Purity ≥98%
  • MDL No. MFCD12756122
  • 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 (3R,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 bench-stable tert-butyl carbamate protecting group and a fluorinated ring system, enabling direct incorporation into complex scaffolds. The (3R,4R) stereochemistry ensures predictable diastereoselective transformations in medicinal chemistry workflows.

Application

(3R,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 fluorine substituent enable selective functionalization, while the tert-butyl carbamate group offers stability and ease of removal under mild acidic conditions. This compound facilitates efficient access to complex nitrogen-containing heterocycles and is well-suited for iterative synthesis workflows requiring orthogonal reactivity and bench-stable intermediates.

Safety Information

Download SDS
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

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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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