N-Benzylquinidinium Chloride [Chiral Phase-Transfer Catalyst]
98.0 %
- Product Code: 71252
CAS:
77481-82-4
| Molecular Weight: | 451.01 g./mol | Molecular Formula: | C₂₇H₃₁ClN₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00198106 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
N-Benzylquinidinium Chloride is widely used as a chiral phase-transfer catalyst in asymmetric synthesis. It facilitates the enantioselective alkylation of various substrates, enabling the production of chiral molecules with high optical purity. This catalyst is particularly effective in the synthesis of amino acids, where it helps create enantiomerically pure compounds crucial for pharmaceuticals. It is also employed in the asymmetric synthesis of complex organic molecules, including natural products and biologically active compounds. Its ability to induce chirality in reactions makes it valuable in the development of drugs, agrochemicals, and fine chemicals, where stereochemistry plays a critical role in efficacy and safety.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to Orange to Green powder to crystal |
| PURITY | 97.5-100 |
| Specific rotation a20DC0.64 H2O | 200-+230 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿11,460.00 |
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N-Benzylquinidinium Chloride [Chiral Phase-Transfer Catalyst]
N-Benzylquinidinium Chloride is widely used as a chiral phase-transfer catalyst in asymmetric synthesis. It facilitates the enantioselective alkylation of various substrates, enabling the production of chiral molecules with high optical purity. This catalyst is particularly effective in the synthesis of amino acids, where it helps create enantiomerically pure compounds crucial for pharmaceuticals. It is also employed in the asymmetric synthesis of complex organic molecules, including natural products and biologically active compounds. Its ability to induce chirality in reactions makes it valuable in the development of drugs, agrochemicals, and fine chemicals, where stereochemistry plays a critical role in efficacy and safety.
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