N-[(1R,2R)-2-(Dimethylamino)cyclohexyl]-N'-[(1R,2S)-2-hydroxy-1,2-diphenylethyl]thiourea
≥98%,99%e.e.
- Product Code: 70667
CAS:
1046493-36-0
| Molecular Weight: | 397.6 g./mol | Molecular Formula: | C₂₃H₃₁N₃OS |
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| EC Number: | MDL Number: | ||
| Melting Point: | 64-66 °C | Boiling Point: | 541.5±60.0 °C |
| Density: | 1.17±0.1 g/mL | Storage Condition: | room temperature, dry |
Product Description:
This compound is primarily utilized as a chiral catalyst in asymmetric synthesis, particularly in enantioselective reactions. Its structure allows it to effectively induce chirality in various organic transformations, such as the addition of nucleophiles to carbonyl compounds or the reduction of ketones. It is often employed in the pharmaceutical industry to produce enantiomerically pure drugs, ensuring higher efficacy and reduced side effects. Additionally, it finds application in academic research for developing new methodologies in stereochemistry and exploring novel catalytic processes. Its thiourea moiety enhances its ability to form hydrogen bonds, making it effective in activating substrates and stabilizing transition states during reactions.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿27,610.00 |
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N-[(1R,2R)-2-(Dimethylamino)cyclohexyl]-N'-[(1R,2S)-2-hydroxy-1,2-diphenylethyl]thiourea
This compound is primarily utilized as a chiral catalyst in asymmetric synthesis, particularly in enantioselective reactions. Its structure allows it to effectively induce chirality in various organic transformations, such as the addition of nucleophiles to carbonyl compounds or the reduction of ketones. It is often employed in the pharmaceutical industry to produce enantiomerically pure drugs, ensuring higher efficacy and reduced side effects. Additionally, it finds application in academic research for developing new methodologies in stereochemistry and exploring novel catalytic processes. Its thiourea moiety enhances its ability to form hydrogen bonds, making it effective in activating substrates and stabilizing transition states during reactions.
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