(R)-2-(Bis(3,5-bis(trifluoromethyl)phenyl)((triethylsilyl)oxy)methyl)pyrrolidine
98%
- Product Code: 51897
CAS:
1061307-56-9
| Molecular Weight: | 639.5900 g./mol | Molecular Formula: | C₂₇H₂₉F₁₂NOSi |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD27975624 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in asymmetric synthesis, particularly as a chiral catalyst or ligand in organic reactions. Its unique structure, featuring trifluoromethyl groups and a triethylsilyl moiety, enhances its steric and electronic properties, making it highly effective in enantioselective transformations. It is often employed in the synthesis of complex molecules, including pharmaceuticals, where precise control over stereochemistry is crucial. Additionally, its stability and reactivity under various conditions make it a valuable tool in the development of new synthetic methodologies, especially in the formation of carbon-carbon and carbon-heteroatom bonds.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿3,393.00 |
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(R)-2-(Bis(3,5-bis(trifluoromethyl)phenyl)((triethylsilyl)oxy)methyl)pyrrolidine
This compound is primarily utilized in asymmetric synthesis, particularly as a chiral catalyst or ligand in organic reactions. Its unique structure, featuring trifluoromethyl groups and a triethylsilyl moiety, enhances its steric and electronic properties, making it highly effective in enantioselective transformations. It is often employed in the synthesis of complex molecules, including pharmaceuticals, where precise control over stereochemistry is crucial. Additionally, its stability and reactivity under various conditions make it a valuable tool in the development of new synthetic methodologies, especially in the formation of carbon-carbon and carbon-heteroatom bonds.
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