2,8-Diazabicyclo[4.3.0]nonane CAS:151213-42-2
The presence of two nitrogen atoms within the ring system allows DBN to act as a bidentate ligand, capable of coordinating to metal ions through both nitrogen atoms. This characteristic makes DBN particularly useful in the preparation of metal complexes, where it can stabilize the metal center and modulate its reactivity. In organic synthesis, DBN serves as a mild base, often used to deprotonate weak acids or to catalyze certain reactions. Its bulky structure prevents it from engaging in unwanted side reactions, making it a more selective alternative to other bases. Additionally, DBN can undergo ring-opening reactions to form linear or branched amines, which are valuable intermediates in the synthesis of more complex organic molecules. The chemistry of 2,8-diazabicyclo[4.3.0]nonane is rich, with various reactions being developed to exploit its独特 properties. Researchers continue to explore new applications for DBN in the fields of catalysis, materials science, and medicine, where its ability to interact with biological systems could lead to the development of novel therapeutics.
Composition | C7H14N2 |
Assay | 99% |
Appearance | white powder |
CAS No. | 151213-42-2 |
Packing | Small and bulk |
Shelf Life | 2 years |
Storage | Store in cool and dry area |
Certification | ISO. |