N1,N2-Dibenzylideneethane-1,2-diamine
≥95%
- Product Code: 54532
CAS:
104-71-2
| Molecular Weight: | 236.31 g./mol | Molecular Formula: | C₁₆H₁₆N₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00022040 | |
| Melting Point: | Boiling Point: | 373.4°C at 760 mmHg | |
| Density: | 0.97g/cm3 | Storage Condition: | 2-8°C, dry and sealed away from light |
Product Description:
N1,N2-Dibenzylideneethane-1,2-diamine is widely used as a ligand in coordination chemistry, forming stable complexes with various transition metals. These complexes are essential in catalytic processes, particularly in asymmetric synthesis, where they help in producing chiral molecules with high enantioselectivity. Additionally, it is employed in organic synthesis as a building block for constructing more complex organic compounds. Its ability to act as a chelating agent makes it valuable in the development of metal-organic frameworks (MOFs) and other advanced materials. In research, it serves as a model compound for studying Schiff base reactions and their applications in material science and catalysis.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White Solid |
| PURITY | 94.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | $72.69 |
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| 1.000 | 10-20 days | $231.58 |
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N1,N2-Dibenzylideneethane-1,2-diamine
N1,N2-Dibenzylideneethane-1,2-diamine is widely used as a ligand in coordination chemistry, forming stable complexes with various transition metals. These complexes are essential in catalytic processes, particularly in asymmetric synthesis, where they help in producing chiral molecules with high enantioselectivity. Additionally, it is employed in organic synthesis as a building block for constructing more complex organic compounds. Its ability to act as a chelating agent makes it valuable in the development of metal-organic frameworks (MOFs) and other advanced materials. In research, it serves as a model compound for studying Schiff base reactions and their applications in material science and catalysis.
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