CAS 286947-16-8
:3,9-Diazabicyclo[4.2.1]nonane-3-carboxylic acid, 1,1-dimethylethylester
Description:
3,9-Diazabicyclo[4.2.1]nonane-3-carboxylic acid, 1,1-dimethylethyl ester, commonly referred to as a bicyclic amine derivative, exhibits unique structural and chemical characteristics due to its bicyclic framework and functional groups. This compound features a diazabicyclic structure, which contributes to its potential as a ligand in coordination chemistry and as a catalyst in various organic reactions. The presence of the carboxylic acid ester functional group enhances its reactivity and solubility in organic solvents, making it useful in synthetic applications. Additionally, the tert-butyl ester group provides steric hindrance, which can influence the compound's reactivity and stability. The compound is likely to exhibit basic properties due to the nitrogen atoms in the bicyclic structure, which can participate in protonation and coordination with metal ions. Overall, its unique structural features and functional groups make it a compound of interest in both academic research and industrial applications, particularly in the fields of organic synthesis and catalysis.
Formula:C12H22N2O2
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Found 4 products.
3,9-Diazabicyclo[4.2.1]nonane-3-carboxylic acid, 1,1-dimethylethyl ester
CAS:Formula:C12H22N2O2Purity:97%Color and Shape:SolidMolecular weight:226.3153tert-Butyl 3,9-diazabicyclo[4.2.1]nonane-3-carboxylate
CAS:<p>tert-Butyl 3,9-diazabicyclo[4.2.1]nonane-3-carboxylate</p>Molecular weight:226.31528g/moltert-butyl 3,9-diazabicyclo[4.2.1]nonane-3-carboxylate
CAS:Formula:C12H22N2O2Purity:97%Color and Shape:Liquid, No data available.Molecular weight:226.32tert-butyl 3,9-diazabicyclo[4.2.1]nonane-3-carboxylate
CAS:<p>Versatile small molecule scaffold</p>Formula:C12H22N2O2Purity:Min. 95%Molecular weight:226.3 g/mol




