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Tert-butyl (S)-3-amino-1-oxa-8-azaspiro[4.5]Decane-8-carboxylate

  • CAS No. 2387567-25-9

  • Cat. No. CS-0471011
  • Purity≥98%
  • MDL No.None

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

Tert-butyl (S)-3-amino-1-oxa-8-azaspiro[4.5]Decane-8-carboxylate|CS-0471011

Structure of 2387567-25-9

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General Information

  • CAS No. 2387567-25-9
  • Cat. No. CS-0471011
  • Purity ≥98%
  • MDL No. None
  • Storage 4°C, protect from light
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₃H₂₄N₂O₃
  • Molecular Weight 256.34
  • Synonym(s) None
  • SMILES CC(C)(C)OC(=O)N1CCC2(CC1)C[C@H](N)CO2

Description

Tert-butyl (S)-3-amino-1-oxa-8-azaspiro[4.5]decane-8-carboxylate is a stereochemically defined spirocyclic amino ester featuring a constrained 8-azaspiro[4.5]decane core with a bench-stable tert-butyl carbamate protecting group. This scaffold integrates a primary amine and a labile ester moiety, enabling selective functionalization in complex molecule synthesis. The spiro architecture imparts rigidity, enhancing conformational control in target-directed discovery.

Application

Tert-butyl (S)-3-amino-1-oxa-8-azaspiro[4.5]decane-8-carboxylate serves as a versatile chiral building block in medicinal chemistry, enabling efficient access to spirocyclic scaffolds prevalent in bioactive molecules. The protected amine and ester functionalities offer orthogonal reactivity, facilitating downstream derivatization via standard coupling, reduction, or cyclization protocols. Bench-stable and readily purified by chromatography, it functions effectively in multistep synthesis of complex heterocycles and API candidates.

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-P330-P362+P364-P405-P501

Quality Control

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Computational Chemistry Data

  • TPSA   64.79
  • LogP   1.5037
  • H_Acceptors   4
  • H_Donors   1
  • Rotatable_Bonds   0

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