(R)-1-[3,5-Bis(trifluoromethyl)phenyl]-3-[1-(dimethylamino)-3-methylbutan-2-yl]thiourea
≥98%,99%e.e.
- Product Code: 70276
CAS:
1048692-61-0
| Molecular Weight: | 401.4 g./mol | Molecular Formula: | C₁₆H₂₁F₆N₃S |
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| Density: | Storage Condition: | room temperature, dry |
Product Description:
This compound is primarily utilized in the field of organic synthesis, particularly as a chiral catalyst or ligand in asymmetric reactions. Its unique structure, featuring trifluoromethyl groups and a thiourea moiety, makes it highly effective in promoting enantioselective transformations, such as the addition of nucleophiles to carbonyl compounds. It is also employed in the development of pharmaceuticals, where its ability to induce chirality is crucial for creating enantiomerically pure drugs. Additionally, it finds use in material science for designing advanced polymers with specific stereochemical properties. Its stability and reactivity under various conditions make it a versatile tool in both academic research and industrial applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.025 | 10-20 days | €66.01 |
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| 0.100 | 10-20 days | €141.99 |
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(R)-1-[3,5-Bis(trifluoromethyl)phenyl]-3-[1-(dimethylamino)-3-methylbutan-2-yl]thiourea
This compound is primarily utilized in the field of organic synthesis, particularly as a chiral catalyst or ligand in asymmetric reactions. Its unique structure, featuring trifluoromethyl groups and a thiourea moiety, makes it highly effective in promoting enantioselective transformations, such as the addition of nucleophiles to carbonyl compounds. It is also employed in the development of pharmaceuticals, where its ability to induce chirality is crucial for creating enantiomerically pure drugs. Additionally, it finds use in material science for designing advanced polymers with specific stereochemical properties. Its stability and reactivity under various conditions make it a versatile tool in both academic research and industrial applications.
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