(1R,2R)-N1,N2-Dimethyl-1,2-bis(3-(trifluoromethyl)phenyl)ethane-1,2-diamine
97%
- Product Code: 36206
CAS:
137944-39-9
| Molecular Weight: | 376.3400 g./mol | Molecular Formula: | C₁₈H₁₈F₆N₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00075560 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the field of asymmetric synthesis and catalysis, particularly in the development of chiral ligands for transition metal catalysts. Its unique structure, featuring trifluoromethyl groups and a chiral diamine backbone, makes it highly effective in facilitating enantioselective reactions, such as hydrogenation, addition, and coupling reactions. These reactions are crucial in the production of pharmaceuticals, agrochemicals, and fine chemicals, where achieving high enantiomeric purity is essential. Additionally, its stability and ability to form strong complexes with metals enhance its utility in creating efficient and selective catalytic systems.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿5,760.00 |
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(1R,2R)-N1,N2-Dimethyl-1,2-bis(3-(trifluoromethyl)phenyl)ethane-1,2-diamine
This compound is primarily utilized in the field of asymmetric synthesis and catalysis, particularly in the development of chiral ligands for transition metal catalysts. Its unique structure, featuring trifluoromethyl groups and a chiral diamine backbone, makes it highly effective in facilitating enantioselective reactions, such as hydrogenation, addition, and coupling reactions. These reactions are crucial in the production of pharmaceuticals, agrochemicals, and fine chemicals, where achieving high enantiomeric purity is essential. Additionally, its stability and ability to form strong complexes with metals enhance its utility in creating efficient and selective catalytic systems.
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