(S)-()-2，2-Dimethyl-4-(hydroxymethyl)-1，3-dioxolane-p-toluenesulfonate
98%
- Product Code: 76940
CAS:
23735-43-5
| Molecular Weight: | 286.34 g./mol | Molecular Formula: | C₁₃H₁₈O₅S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00063234 | |
| Melting Point: | 25°C (凝固点) | Boiling Point: | |
| Density: | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily used as a chiral building block in organic synthesis, particularly in the production of pharmaceuticals and fine chemicals. Its structure, featuring a dioxolane ring and a hydroxymethyl group, makes it valuable for constructing complex molecules with specific stereochemistry. It is often employed in the synthesis of enantiomerically pure compounds, where its tosylate group acts as a good leaving group, facilitating nucleophilic substitution reactions. Additionally, it is utilized in the development of antiviral and anticancer agents, where precise stereochemical control is crucial for biological activity. Its stability and reactivity also make it suitable for use in asymmetric synthesis and as an intermediate in the preparation of chiral ligands or catalysts.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Light yellow to yellow Liquid |
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿2,880.00 |
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| 5.000 | 10-20 days | ฿12,460.00 |
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(S)-()-2，2-Dimethyl-4-(hydroxymethyl)-1，3-dioxolane-p-toluenesulfonate
This chemical is primarily used as a chiral building block in organic synthesis, particularly in the production of pharmaceuticals and fine chemicals. Its structure, featuring a dioxolane ring and a hydroxymethyl group, makes it valuable for constructing complex molecules with specific stereochemistry. It is often employed in the synthesis of enantiomerically pure compounds, where its tosylate group acts as a good leaving group, facilitating nucleophilic substitution reactions. Additionally, it is utilized in the development of antiviral and anticancer agents, where precise stereochemical control is crucial for biological activity. Its stability and reactivity also make it suitable for use in asymmetric synthesis and as an intermediate in the preparation of chiral ligands or catalysts.
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