1-((1R,2R)-2-(Dimethylamino)-1,2-diphenylethyl)-3-((S)-1-(naphthalen-1-yl)ethyl)thiourea
97%
- Product Code: 70555
CAS:
2459946-48-4
| Molecular Weight: | 453.64 g./mol | Molecular Formula: | C₂₉H₃₁N₃S |
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| Density: | Storage Condition: | 2-8°C, protected from light, inert gas |
Product Description:
This compound is primarily utilized in asymmetric synthesis and catalysis, particularly in enantioselective reactions. Its structure, featuring chiral centers and a thiourea group, makes it effective as a chiral ligand or catalyst in organic transformations. It is often employed in the synthesis of complex molecules, including pharmaceuticals, where high enantiomeric purity is required. The compound's ability to induce chirality in substrates is valuable in producing optically active intermediates or final products. Additionally, it has been explored in the development of novel catalytic systems for C-C bond formation and other stereospecific reactions. Its application extends to academic research in asymmetric catalysis, aiding in the discovery of new methodologies for efficient and selective synthesis.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | ฿5,040.00 |
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1-((1R,2R)-2-(Dimethylamino)-1,2-diphenylethyl)-3-((S)-1-(naphthalen-1-yl)ethyl)thiourea
This compound is primarily utilized in asymmetric synthesis and catalysis, particularly in enantioselective reactions. Its structure, featuring chiral centers and a thiourea group, makes it effective as a chiral ligand or catalyst in organic transformations. It is often employed in the synthesis of complex molecules, including pharmaceuticals, where high enantiomeric purity is required. The compound's ability to induce chirality in substrates is valuable in producing optically active intermediates or final products. Additionally, it has been explored in the development of novel catalytic systems for C-C bond formation and other stereospecific reactions. Its application extends to academic research in asymmetric catalysis, aiding in the discovery of new methodologies for efficient and selective synthesis.
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