3-Amino-3-azabicyclo[3.3.0]octane CAS:58108-05-7
3-Amino-3-azabicyclo[3.3.0]octane finds diverse applications across different fields: Medicinal Chemistry: AABCO derivatives serve as scaffolds or building blocks in medicinal chemistry for the synthesis of biologically active molecules. Their rigid bicyclic structure and amino functionality make them valuable in the design and optimization of pharmaceutical compounds targeting various biological pathways and diseases. Catalysis: AABCO-containing compounds act as catalysts or ligands in catalytic reactions, particularly in asymmetric synthesis and organocatalysis. Their chiral nature and unique stereochemistry enable the control of reaction outcomes, facilitating the synthesis of enantioenriched compounds with high efficiency and selectivity. Materials Science: AABCO derivatives are utilized in the synthesis of functional materials such as polymers, dendrimers, and coordination complexes. Their versatile reactivity allows for the incorporation of AABCO motifs into macromolecular structures, imparting desired properties such as solubility, conductivity, or optical activity. Drug Delivery Systems: AABCO-based compounds are employed in the development of drug delivery systems for controlled release and targeted delivery of therapeutics. By conjugating drugs or targeting ligands to AABCO-modified carriers, researchers can enhance drug stability, improve pharmacokinetics, and achieve site-specific delivery, leading to enhanced therapeutic efficacy and reduced side effects. Organic Synthesis: AABCO serves as a key intermediate in organic synthesis, particularly in the preparation of complex molecules and natural products. Its bicyclic structure and amino functionality enable diverse synthetic transformations, allowing for the efficient construction of structurally intricate compounds with potential biological activities. Biological Probes: AABCO derivatives are utilized as molecular probes in biochemical and pharmacological research for studying receptor-ligand interactions, enzyme mechanisms, and cellular processes. By incorporating AABCO motifs into probe molecules, researchers can modulate their binding affinity, specificity, and cellular uptake, enabling investigations into biological phenomena and drug discovery efforts. In conclusion, 3-Amino-3-azabicyclo[3.3.0]octane exhibits versatile applications in medicinal chemistry, catalysis, materials science, drug delivery, organic synthesis, and biological research. Its unique bicyclic structure and amino functionality make it a valuable scaffold, catalyst, building block, and probe in various scientific and industrial endeavors, driving advancements in multiple disciplines.
Composition | C6H12N2 |
Assay | 99% |
Appearance | white powder |
CAS No. | 58108-05-7 |
Packing | Small and bulk |
Shelf Life | 2 years |
Storage | Store in cool and dry area |
Certification | ISO. |