(1R,2S,5R)-(-)-Menthyl (S)-p-toluenesulfinate
98%
- Product Code: 70786
Alias:
(1R,2S,5R)-(-)-Menthol (S)-p-toluenesulfinate (-)-(1R)-menthyl (S)-p-toluenesulfinate (S)-(- )-menthyl p-toluene sulfinate
CAS:
1517-82-4
| Molecular Weight: | 294.45 g./mol | Molecular Formula: | C₁₇H₂₆O₂S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00010192 | |
| Melting Point: | 99-104 °C | Boiling Point: | |
| Density: | 1.08 | Storage Condition: | -20°C |
Product Description:
This compound is primarily used as a chiral auxiliary in asymmetric synthesis, particularly in the formation of enantiomerically pure compounds. It is employed in the synthesis of pharmaceuticals and fine chemicals where the control of stereochemistry is crucial. The compound's ability to induce chirality in reactions makes it valuable in producing optically active intermediates. Additionally, it is utilized in the preparation of chiral sulfoxides, which are important in medicinal chemistry and drug development. Its application extends to catalysis, where it aids in achieving high enantioselectivity in various organic transformations.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to light yellow Crystalline powder |
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿990.00 |
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| 5.000 | 10-20 days | ฿3,520.00 |
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(1R,2S,5R)-(-)-Menthyl (S)-p-toluenesulfinate
This compound is primarily used as a chiral auxiliary in asymmetric synthesis, particularly in the formation of enantiomerically pure compounds. It is employed in the synthesis of pharmaceuticals and fine chemicals where the control of stereochemistry is crucial. The compound's ability to induce chirality in reactions makes it valuable in producing optically active intermediates. Additionally, it is utilized in the preparation of chiral sulfoxides, which are important in medicinal chemistry and drug development. Its application extends to catalysis, where it aids in achieving high enantioselectivity in various organic transformations.
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