(R)-()-2,2-Dimethyl-1,3-dioxolane-4-carboxaldehyde
50% in Dichloromethane
- Product Code: 229965
CAS:
15186-48-8
| Molecular Weight: | 130.14 g./mol | Molecular Formula: | C₆H₁₀O₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00269682 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | -20℃ |
Product Description:
Used as a chiral building block in the synthesis of pharmaceuticals and natural products. Its aldehyde functionality allows for easy transformation into various functional groups such as alcohols, amines, or carboxylic acids, making it valuable in asymmetric synthesis. Commonly employed in the preparation of bioactive molecules where stereochemistry is critical, such as antiviral or antitumor agents. The dioxolane ring acts as a protecting group for carbonyls while also serving as a rigid scaffold to control stereoselectivity in downstream reactions. Frequently utilized in multi-step organic syntheses requiring high enantiomeric purity.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 5.000 | 10-20 days | ฿300.00 |
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| 25.000 | 10-20 days | ฿790.00 |
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| 100.000 | 10-20 days | ฿2,960.00 |
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| 500.000 | 10-20 days | ฿13,250.00 |
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(R)-()-2,2-Dimethyl-1,3-dioxolane-4-carboxaldehyde
Used as a chiral building block in the synthesis of pharmaceuticals and natural products. Its aldehyde functionality allows for easy transformation into various functional groups such as alcohols, amines, or carboxylic acids, making it valuable in asymmetric synthesis. Commonly employed in the preparation of bioactive molecules where stereochemistry is critical, such as antiviral or antitumor agents. The dioxolane ring acts as a protecting group for carbonyls while also serving as a rigid scaffold to control stereoselectivity in downstream reactions. Frequently utilized in multi-step organic syntheses requiring high enantiomeric purity.
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