1-(Tert-butyl) 2-methyl (2S)-5-allylpyrrolidine-1,2-dicarboxylate
95%
- Product Code: 82991
CAS:
195964-65-9
| Molecular Weight: | 269.34 g./mol | Molecular Formula: | C₁₄H₂₃NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD16877486 | |
| Melting Point: | Boiling Point: | 328.9±35.0 °C(Predicted) | |
| Density: | 1.061±0.06 g/cm3(Predicted) | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in organic synthesis as a chiral building block. Its structure, featuring both a tert-butyl group and an allyl group, makes it valuable in the preparation of complex molecules, particularly in pharmaceutical research. The compound is often employed in the synthesis of pyrrolidine-based frameworks, which are common in bioactive molecules and drug candidates. Its stereochemistry allows for the creation of enantiomerically pure products, which is crucial in the development of therapeutic agents with specific biological activities. Additionally, the allyl group provides a handle for further functionalization through reactions like cross-coupling or olefin metathesis, enhancing its versatility in synthetic applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $470.12 |
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| 0.250 | 10-20 days | $881.47 |
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| 1.000 | 10-20 days | $1,762.93 |
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1-(Tert-butyl) 2-methyl (2S)-5-allylpyrrolidine-1,2-dicarboxylate
This compound is primarily utilized in organic synthesis as a chiral building block. Its structure, featuring both a tert-butyl group and an allyl group, makes it valuable in the preparation of complex molecules, particularly in pharmaceutical research. The compound is often employed in the synthesis of pyrrolidine-based frameworks, which are common in bioactive molecules and drug candidates. Its stereochemistry allows for the creation of enantiomerically pure products, which is crucial in the development of therapeutic agents with specific biological activities. Additionally, the allyl group provides a handle for further functionalization through reactions like cross-coupling or olefin metathesis, enhancing its versatility in synthetic applications.
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