(4S,5S)-2,2-Dimethyl-α,α,α',α'-tetra(1-naphthyl)-1,3-dioxolane-4,5-dimethanol
≥95%,≥99%e.e.
- Product Code: 59740
CAS:
171086-52-5
| Molecular Weight: | 666.8 g./mol | Molecular Formula: | C₄₇H₃₈O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 201°C | |
| Density: | Storage Condition: | room temperature, dry |
Product Description:
This chemical is primarily utilized in asymmetric synthesis as a chiral auxiliary or ligand. Its unique structure, featuring multiple naphthyl groups, makes it highly effective in inducing chirality in organic reactions, particularly in stereoselective transformations. It is often employed in catalytic systems to enhance enantioselectivity in the synthesis of complex molecules, such as pharmaceuticals or fine chemicals. The compound’s rigid framework and steric properties allow for precise control over the spatial arrangement of reactants, leading to the formation of specific enantiomers with high purity. Additionally, it can be used in the development of chiral catalysts for applications in industrial chemical processes, where achieving high enantiomeric excess is critical. Its role in facilitating asymmetric hydrogenation, epoxidation, and other key reactions makes it a valuable tool in synthetic organic chemistry.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | solid |
| PURITY | 94.5-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.200 | 10-20 days | ฿800.00 |
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| 1.000 | 10-20 days | ฿2,600.00 |
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| 5.000 | 10-20 days | ฿9,650.00 |
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(4S,5S)-2,2-Dimethyl-α,α,α',α'-tetra(1-naphthyl)-1,3-dioxolane-4,5-dimethanol
This chemical is primarily utilized in asymmetric synthesis as a chiral auxiliary or ligand. Its unique structure, featuring multiple naphthyl groups, makes it highly effective in inducing chirality in organic reactions, particularly in stereoselective transformations. It is often employed in catalytic systems to enhance enantioselectivity in the synthesis of complex molecules, such as pharmaceuticals or fine chemicals. The compound’s rigid framework and steric properties allow for precise control over the spatial arrangement of reactants, leading to the formation of specific enantiomers with high purity. Additionally, it can be used in the development of chiral catalysts for applications in industrial chemical processes, where achieving high enantiomeric excess is critical. Its role in facilitating asymmetric hydrogenation, epoxidation, and other key reactions makes it a valuable tool in synthetic organic chemistry.
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