3-[[3,5-bis(trifluoroMethyl)phenyl]aMino]-4-[(8α,9S)-cinchonan-9-ylaMino]-3-Cyclobutene-1,2-dione
98%
- Product Code: 70632
CAS:
1256245-86-9
Molecular Weight: | 600.5541592 g./mol | Molecular Formula: | C₃₁H₂₆F₆N₄O₂ |
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Density: | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily utilized in the field of organic synthesis and catalysis, particularly in asymmetric synthesis reactions. Its unique structure, featuring a cinchona alkaloid derivative, makes it highly effective as a chiral catalyst or ligand in enantioselective transformations. It is often employed in the synthesis of complex organic molecules, where controlling stereochemistry is crucial, such as in the production of pharmaceuticals and fine chemicals. Additionally, its trifluoromethyl groups enhance its stability and reactivity, making it suitable for use in harsh reaction conditions. This compound is also explored in the development of novel catalytic systems for industrial applications, where high selectivity and efficiency are required.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.010 | 10-20 days | ฿5,706.00 |
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0.050 | 10-20 days | ฿22,806.00 |
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3-[[3,5-bis(trifluoroMethyl)phenyl]aMino]-4-[(8α,9S)-cinchonan-9-ylaMino]-3-Cyclobutene-1,2-dione
This chemical is primarily utilized in the field of organic synthesis and catalysis, particularly in asymmetric synthesis reactions. Its unique structure, featuring a cinchona alkaloid derivative, makes it highly effective as a chiral catalyst or ligand in enantioselective transformations. It is often employed in the synthesis of complex organic molecules, where controlling stereochemistry is crucial, such as in the production of pharmaceuticals and fine chemicals. Additionally, its trifluoromethyl groups enhance its stability and reactivity, making it suitable for use in harsh reaction conditions. This compound is also explored in the development of novel catalytic systems for industrial applications, where high selectivity and efficiency are required.
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