(11R,12R)-9,10-Dihydro-9,10-ethanoanthracene-11,12-diamine
98.0%
- Product Code: 70770
CAS:
181139-49-1
| Molecular Weight: | 236.31 g./mol | Molecular Formula: | C₁₆H₁₆N₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09038520 | |
| Melting Point: | 159 °C | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the field of organic synthesis, where it serves as a chiral diamine ligand. Its unique structure makes it valuable in asymmetric catalysis, particularly in reactions that require high enantioselectivity, such as the synthesis of pharmaceuticals and fine chemicals. The rigid ethanoanthracene backbone provides stability and precise spatial arrangement, enhancing its effectiveness in controlling stereochemistry. Additionally, it has been explored in the development of advanced materials, including chiral polymers and coordination complexes, due to its ability to induce specific molecular orientations. Its applications also extend to research in supramolecular chemistry, where it aids in the design of host-guest systems with tailored properties.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White - Pale yellow Crystal - Powder |
| PURITY | 98-100 |
| MELTING POINT | 155-159 |
| Specific rotation a20DC1 methanol | -20--16 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿13,860.00 |
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(11R,12R)-9,10-Dihydro-9,10-ethanoanthracene-11,12-diamine
This compound is primarily utilized in the field of organic synthesis, where it serves as a chiral diamine ligand. Its unique structure makes it valuable in asymmetric catalysis, particularly in reactions that require high enantioselectivity, such as the synthesis of pharmaceuticals and fine chemicals. The rigid ethanoanthracene backbone provides stability and precise spatial arrangement, enhancing its effectiveness in controlling stereochemistry. Additionally, it has been explored in the development of advanced materials, including chiral polymers and coordination complexes, due to its ability to induce specific molecular orientations. Its applications also extend to research in supramolecular chemistry, where it aids in the design of host-guest systems with tailored properties.
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