2,8,9-Triisopropyl-2,5,8,9-tetraaza-1-phosphabicyclo[3,3,3]undecane
- Product Code: 78380
Alias:
[2,5,8,9-Tetraaza-1-phosphabicyclo[3.3.3]undecane-2,8,9-tri(1-methylethyl)]
CAS:
175845-21-3
| Molecular Weight: | 300.42 g./mol | Molecular Formula: | C₁₅H₃₃N₄P |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD03701530 | |
| Melting Point: | Boiling Point: | 351.4ºC at 760 mmHg | |
| Density: | 0.922 g/mL | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized as a ligand in coordination chemistry, particularly in the formation of complexes with transition metals. Its unique bicyclic structure and nitrogen-phosphorus framework make it highly effective in stabilizing metal centers, which is crucial in catalytic processes. It is often employed in homogeneous catalysis, where it enhances the efficiency and selectivity of reactions such as hydrogenation, hydroformylation, and cross-coupling reactions. Additionally, its steric and electronic properties are leveraged in the development of advanced materials and in the study of organometallic chemistry, contributing to innovations in industrial and academic research.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | White to Yellow (Moist Crystalline Solid) or Colorless to Yellow (Liquid) |
| Infrared spectrum | Conforms to Structure |
| Proton NMR spectra | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿5,868.00 |
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2,8,9-Triisopropyl-2,5,8,9-tetraaza-1-phosphabicyclo[3,3,3]undecane
This chemical is primarily utilized as a ligand in coordination chemistry, particularly in the formation of complexes with transition metals. Its unique bicyclic structure and nitrogen-phosphorus framework make it highly effective in stabilizing metal centers, which is crucial in catalytic processes. It is often employed in homogeneous catalysis, where it enhances the efficiency and selectivity of reactions such as hydrogenation, hydroformylation, and cross-coupling reactions. Additionally, its steric and electronic properties are leveraged in the development of advanced materials and in the study of organometallic chemistry, contributing to innovations in industrial and academic research.
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