(R)-4-(2-Hydroxyethyl)-2,2-diisopropyl-1,3-dioxolane
95%
- Product Code: 64168
CAS:
1820574-15-9
| Molecular Weight: | 202.29 g./mol | Molecular Formula: | C₁₁H₂₂O₃ |
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| Density: | 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 chiral building block for the production of enantiomerically pure compounds, which are crucial in the development of drugs with specific biological activities. Its structure, featuring a dioxolane ring and a hydroxyethyl group, makes it a valuable intermediate in asymmetric synthesis. Additionally, it is employed in the preparation of ligands for catalysis, enhancing the efficiency and selectivity of various chemical reactions. Its stability and reactivity also make it suitable for use in fine chemical manufacturing and research applications where precise molecular control is required.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Colorless - Almost colorless Liquid |
| PURITY | 94.5-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.200 | 10-20 days | ฿3,290.00 |
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(R)-4-(2-Hydroxyethyl)-2,2-diisopropyl-1,3-dioxolane
This chemical is primarily utilized in the synthesis of complex organic molecules, particularly in the pharmaceutical industry. It serves as a chiral building block for the production of enantiomerically pure compounds, which are crucial in the development of drugs with specific biological activities. Its structure, featuring a dioxolane ring and a hydroxyethyl group, makes it a valuable intermediate in asymmetric synthesis. Additionally, it is employed in the preparation of ligands for catalysis, enhancing the efficiency and selectivity of various chemical reactions. Its stability and reactivity also make it suitable for use in fine chemical manufacturing and research applications where precise molecular control is required.
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