N-Boc-9-azabicyclo[3.3.1]nonan-3-one is a bicyclic compound characterized by its unique structure, which includes a bicyclo[3.3.1] framework and a nitrogen atom incorporated into the ring system. The "N-Boc" designation indicates that the nitrogen atom is protected by a tert-butyloxycarbonyl (Boc) group, which is commonly used in organic synthesis to temporarily protect amines. This compound features a ketone functional group at the 3-position of the bicyclic structure, contributing to its reactivity and potential applications in medicinal chemistry. The bicyclic nature of the compound provides rigidity, which can influence its biological activity and interaction with other molecules. N-Boc-9-azabicyclo[3.3.1]nonan-3-one is often utilized in the synthesis of various pharmaceuticals and bioactive compounds, making it of interest in drug development and research. Its specific properties, such as solubility and stability, can vary depending on the conditions and solvents used in experiments.

N-Boc-9-azabicyclo[3.3.1]nonan-3-one

512822-27-4: 9-Azabicyclo[3.3.1]nonane-9-carboxylic acid, 3-oxo-, 1,1-dimethylethyl ester, tert-Butyl 3-oxo-9-azabicyclo[3.3.1]nonane-9-carboxylate, Tert-Butyl 7-Oxo-9-Azabicyclo[3.3.1]Nonane-9-Carboxylate, 9-Boc-3-Oxo-9-Azabicyclo[3.3.1]Nonane

N-Boc-9-Azabicyclo[3.3.1]nonan-3-one

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9-Azabicyclo[3.3.1]nonan-3-one, N-BOC protected

CAS 512822-27-4: N-Boc-9-azabicyclo[3.3.1]nonan-3-one

N-Boc-9-Azabicyclo[3.3.1]nonan-3-one

Ref: 10-F093587

N-Boc-9-Azabicyclo[3.3.1]nonan-3-one

Ref: IN-DA003STM

N-Boc-9-Azabicyclo[3.3.1]nonan-3-one

Ref: 3D-FB32840

9-Azabicyclo[3.3.1]nonan-3-one, N-BOC protected

Ref: 54-OR952038