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tert-Butyl rel-(1R,5S,6S)-6-amino-3-azabicyclo[3.1.0]hexane-3-carboxylate

  • CAS No. 273206-92-1

  • Cat. No. CS-0036945
  • Purity≥95%
  • MDL No.MFCD09832898

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

tert-Butyl rel-(1R,5S,6S)-6-amino-3-azabicyclo[3.1.0]hexane-3-carboxylate|CS-0036945

Structure of 273206-92-1

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General Information

  • CAS No. 273206-92-1
  • Cat. No. CS-0036945
  • Purity ≥95%
  • MDL No. MFCD09832898
  • Storage 4°C, protect from light
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₀H₁₈N₂O₂
  • Molecular Weight None
  • Synonym(s) (1α,5α,6α)-6-Amino-3-azabicyclo[3.1.0]hexane-3-carboxylic Acid 1,1-Dimethylethyl Ester
  • SMILES N[C@H]1[C@@]2([H])[C@]1([H])CN(C2)C(OC(C)(C)C)=O

Description

tert-Butyl rel-(1R,5S,6S)-6-amino-3-azabicyclo[3.1.0]hexane-3-carboxylate features a rigid bicyclic scaffold with defined stereochemistry, enabling precise spatial control in medicinal chemistry applications. The tert-butyl ester group enhances solubility and stability during synthesis, while the primary amine supports direct derivatization. This configuration delivers high fidelity in target engagement for CNS-directed drug discovery projects.

Application

tert-Butyl rel-(1R,5S,6S)-6-amino-3-azabicyclo[3.1.0]hexane-3-carboxylate serves as a conformationally constrained, enantiopure building block for medicinal chemistry and natural product synthesis. The bicyclic scaffold imparts rigidity to modulate target binding affinity, while the protected amine and carboxylate functionalities enable sequential functionalization. Bench-stable and compatible with standard peptide coupling and reductive amination protocols, it facilitates efficient access to complex heterocyclic architectures and API intermediates.

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

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Computational Chemistry Data

  • TPSA   55.56
  • LogP   0.8104
  • H_Acceptors   3
  • H_Donors   1
  • Rotatable_Bonds   0

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