(-)-Methyl (S)-2,2-dimethyl-1,3-dioxolane-4-carboxylate
96%
- Product Code: 205174
Alias:
α,β-isopropylene-L-glycerate; methyl 2,3-O-isopropylene-L-glycerate; methyl α,β-isopropylene-L-glycerate
CAS:
60456-21-5
| Molecular Weight: | 160.17 g./mol | Molecular Formula: | C₇H₁₂O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00066526 | |
| Melting Point: | Boiling Point: | 84-86 °C15 mm Hg(lit.) | |
| Density: | 1.106 g/mL at 25 °C(lit.) | Storage Condition: | 2~8°C |
Product Description:
Used as a chiral building block in the synthesis of biologically active compounds, particularly in pharmaceuticals and agrochemicals. Its cyclic acetonide structure provides stereochemical control during reactions, making it valuable in asymmetric synthesis. Commonly employed to introduce chirality in the development of enantiomerically pure drugs. Also utilized in the preparation of natural products and intermediates where stereoselectivity is critical. The compound’s stability and reactivity profile make it suitable for multi-step synthetic routes.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 1g | 10-20 days | ฿790.00 |
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| 5g | 10-20 days | ฿3,010.00 |
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| 100g | 10-20 days | ฿54,990.00 |
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| 25g | 10-20 days | ฿14,690.00 |
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(-)-Methyl (S)-2,2-dimethyl-1,3-dioxolane-4-carboxylate
Used as a chiral building block in the synthesis of biologically active compounds, particularly in pharmaceuticals and agrochemicals. Its cyclic acetonide structure provides stereochemical control during reactions, making it valuable in asymmetric synthesis. Commonly employed to introduce chirality in the development of enantiomerically pure drugs. Also utilized in the preparation of natural products and intermediates where stereoselectivity is critical. The compound’s stability and reactivity profile make it suitable for multi-step synthetic routes.
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