Atomfair

Awaiting product image

Atomfair tert-Butyl 3,9-diazabicyclo[4.2.1]nonane-9-carboxylate C12H22N2O2

Description tert-Butyl 3,9-diazabicyclo[4.2.1]nonane-9-carboxylate (CAS: 1251015-63-0) is a high-purity bicyclic amine derivative with the molecular formula C12H22N2O2. This compound features a rigid diazabicyclo[4.2.1]nonane core protected by a tert-butyloxycarbonyl (Boc) group, making it a valuable intermediate in organic synthesis and medicinal chemistry. Its unique structure enables applications in the development of pharmaceuticals, agrochemicals, and advanced materials. The product is supplied as a white to off-white crystalline solid with ??95% purity (HPLC), ensuring consistency for research and industrial use. Store under inert conditions at 2-8??C to maintain stability.

Category:
Brands:

Description

Description

tert-Butyl 3,9-diazabicyclo[4.2.1]nonane-9-carboxylate (CAS: 1251015-63-0) is a high-purity bicyclic amine derivative with the molecular formula C12H22N2O2. This compound features a rigid diazabicyclo[4.2.1]nonane core protected by a tert-butyloxycarbonyl (Boc) group, making it a valuable intermediate in organic synthesis and medicinal chemistry. Its unique structure enables applications in the development of pharmaceuticals, agrochemicals, and advanced materials. The product is supplied as a white to off-white crystalline solid with ??95% purity (HPLC), ensuring consistency for research and industrial use. Store under inert conditions at 2-8??C to maintain stability.

  • CAS No: 1251015-63-0
  • Molecular Formula: C12H22N2O2
  • Molecular Weight: 226.32
  • Exact Mass: 226.168127949
  • Monoisotopic Mass: 226.168127949
  • IUPAC Name: tert-butyl 3,9-diazabicyclo[4.2.1]nonane-9-carboxylate
  • SMILES: CC(C)(C)OC(=O)N1C2CCC1CNCC2
  • Synonyms: 1251015-63-0, tert-butyl 3,9-diazabicyclo[4.2.1]nonane-9-carboxylate, DTXSID00679174, tert-Butyl 3,9-diazabicyclo(4.2.1)nonane-9-carboxylate, DTXCID10629923

Application

tert-Butyl 3,9-diazabicyclo[4.2.1]nonane-9-carboxylate is widely utilized as a key building block in the synthesis of complex nitrogen-containing heterocycles. Its Boc-protected amine group facilitates selective deprotection for further functionalization in drug discovery, particularly for CNS-targeting compounds. Researchers also employ this intermediate in the development of catalysts and ligands for asymmetric synthesis.

If you are interested or have any questions, please contact us at support@atomfair.com