(R)-methyl 2-((S)-2,2-dimethyl-1,3-dioxolan-4-yl)-2-(tosyloxy)acetate
95%
- Product Code: 82858
CAS:
166249-17-8
| Molecular Weight: | 344.38 g./mol | Molecular Formula: | C₁₅H₂₀O₇S |
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| EC Number: | MDL Number: | ||
| Melting Point: | 62-63 °C | Boiling Point: | 455.9±35.0 °C(Predicted) |
| Density: | 1.258±0.06 g/cm3(Predicted) | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized in the synthesis of complex organic molecules, particularly in the pharmaceutical industry. It serves as a key intermediate in the production of chiral compounds, which are essential for developing enantiomerically pure drugs. Its structure, featuring a tosyloxy group and a dioxolane ring, makes it valuable for stereoselective reactions, enabling the construction of specific molecular configurations. Additionally, it is employed in asymmetric synthesis to create biologically active compounds, such as antiviral or anticancer agents. Its role in facilitating precise chemical transformations makes it a critical component in advanced medicinal chemistry research.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | €284.93 |
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| 0.250 | 10-20 days | €498.62 |
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| 1.000 | 10-20 days | €997.24 |
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(R)-methyl 2-((S)-2,2-dimethyl-1,3-dioxolan-4-yl)-2-(tosyloxy)acetate
This chemical is primarily utilized in the synthesis of complex organic molecules, particularly in the pharmaceutical industry. It serves as a key intermediate in the production of chiral compounds, which are essential for developing enantiomerically pure drugs. Its structure, featuring a tosyloxy group and a dioxolane ring, makes it valuable for stereoselective reactions, enabling the construction of specific molecular configurations. Additionally, it is employed in asymmetric synthesis to create biologically active compounds, such as antiviral or anticancer agents. Its role in facilitating precise chemical transformations makes it a critical component in advanced medicinal chemistry research.
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