(4S,5R)-Methyl 2,2,5-trimethyl-1,3-dioxolane-4-carboxylate
95%
- Product Code: 234907
CAS:
38410-80-9
| Molecular Weight: | 174.19 g./mol | Molecular Formula: | C₈H₁₄O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 243.8°C | |
| Density: | Storage Condition: | 2-8°C |
Product Description:
Used as a chiral building block in asymmetric synthesis, particularly in the pharmaceutical and fine chemical industries. Its rigid dioxolane ring and defined stereochemistry make it valuable for constructing stereoselective intermediates. Commonly employed in the development of optically active drugs, where it helps control the spatial arrangement of functional groups during multi-step syntheses. Also utilized in the preparation of natural product analogs and bioactive molecules requiring high enantiomeric purity. Its ester functionality allows for easy transformation into acids, alcohols, or amides, enabling further structural diversification.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | ฿1,370.00 |
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| 250mg | 10-20 days | ฿1,710.00 |
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| 1g | 10-20 days | ฿3,610.00 |
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| 5g | 10-20 days | ฿12,940.00 |
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| 25g | 10-20 days | ฿46,390.00 |
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(4S,5R)-Methyl 2,2,5-trimethyl-1,3-dioxolane-4-carboxylate
Used as a chiral building block in asymmetric synthesis, particularly in the pharmaceutical and fine chemical industries. Its rigid dioxolane ring and defined stereochemistry make it valuable for constructing stereoselective intermediates. Commonly employed in the development of optically active drugs, where it helps control the spatial arrangement of functional groups during multi-step syntheses. Also utilized in the preparation of natural product analogs and bioactive molecules requiring high enantiomeric purity. Its ester functionality allows for easy transformation into acids, alcohols, or amides, enabling further structural diversification.
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