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CAS 132234-69-6

:

1,1-Dimethylethyl N-(3-endo)-8-azabicyclo[3.2.1]oct-3-ylcarbamate

Description:
1,1-Dimethylethyl N-(3-endo)-8-azabicyclo[3.2.1]oct-3-ylcarbamate, with the CAS number 132234-69-6, is a chemical compound characterized by its unique bicyclic structure and functional groups. It features a carbamate moiety, which is indicative of its potential biological activity, particularly in the context of pharmacology. The presence of the 8-azabicyclo[3.2.1]octane framework suggests that it may interact with biological systems, possibly as a ligand for receptors or enzymes. The dimethyl substituent contributes to its steric properties, potentially influencing its solubility and reactivity. This compound may exhibit specific stereochemistry due to the bicyclic structure, which can affect its interaction with biological targets. Overall, its characteristics suggest potential applications in medicinal chemistry, although detailed studies would be necessary to elucidate its specific properties, mechanisms of action, and potential therapeutic uses.
Formula:C12H22N2O2
InChI:InChI=1/C12H22N2O2/c1-12(2,3)16-11(15)14-10-6-8-4-5-9(7-10)13-8/h8-10,13H,4-7H2,1-3H3,(H,14,15)/t8-,9+,10+
InChI key:InChIKey=UUHPKKKRSZBQIG-MYJAWHEDNA-N
SMILES:N(C(OC(C)(C)C)=O)[C@H]1C[C@@]2(N[C@](C1)(CC2)[H])[H]
Synonyms:
  • (3-endo)-8-Azabicyclo[3.2.1]oct-3-ylcarbamic acid tert-butyl ester
  • 1,1-Dimethylethyl N-(3-endo)-8-azabicyclo[3.2.1]oct-3-ylcarbamate
  • Carbamic acid, (3-endo)-8-azabicyclo[3.2.1]oct-3-yl-, 1,1-dimethylethyl ester
  • Carbamic acid, 8-azabicyclo[3.2.1]oct-3-yl-, 1,1-dimethylethyl ester, endo-
  • Carbamic acid, N-(3-endo)-8-azabicyclo[3.2.1]oct-3-yl-, 1,1-dimethylethyl ester
  • Endo-3-(Boc-Amino)-8-Azabicyclo[3.2.1]Octane
  • Endo-Tert-Butyl 8-Aza- Bicyclo[3.2.1]Octan-3- Ylcarbamate
  • tert-Butyl N-[(3-endo)-8-azabicyclo[3.2.1]octan-3-yl]carbamate
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