CAS 512822-27-4

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

Description:

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.

Formula: C₁₃H₂₁NO₃

InChI: InChI=1/C13H21NO3/c1-13(2,3)17-12(16)14-9-5-4-6-10(14)8-11(15)7-9/h9-10H,4-8H2,1-3H3

SMILES: CC(C)(C)OC(=O)N1C2CCCC1CC(=O)C2

Synonyms:

• 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

CAS: 512822-27-4

Formula: C₁₃H₂₁NO₃

Purity: 97%

Color and Shape: Solid

Molecular weight: 239.3107

Ref: IN-DA003STM

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

CAS: 512822-27-4

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

Formula: C₁₃H₂₁NO₃

Purity: 98%

Color and Shape: white solid

Molecular weight: 239.31g/mol

Ref: 54-OR952038

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

CAS: 512822-27-4

Formula: C₁₃H₂₁NO₃

Purity: 97%

Color and Shape: Solid

Molecular weight: 239.315

Ref: 10-F093587