(S)-Alpha-allyl-proline, HCl
purum, ≥98.0% (TLC)
- Product Code: 73178
CAS:
129704-91-2
| Molecular Weight: | 191.66 g./mol | Molecular Formula: | C₈H₁₃NO₂HCl |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD06659238 | |
| Melting Point: | 230 - 232 ℃ | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
(S)-Alpha-allyl-proline, HCl is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key chiral building block in the development of peptide-based drugs and bioactive molecules. The compound is often employed in asymmetric synthesis to introduce specific stereochemistry into target molecules, enhancing their biological activity or selectivity. Additionally, it is used in the preparation of proline derivatives, which are essential in designing enzyme inhibitors and receptor modulators. Its application extends to medicinal chemistry, where it aids in the creation of novel therapeutic agents targeting diseases such as cancer, viral infections, and neurological disorders. The allyl group in the structure also allows for further functionalization, making it a versatile intermediate in complex chemical transformations.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $467.06 |
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(S)-Alpha-allyl-proline, HCl
(S)-Alpha-allyl-proline, HCl is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key chiral building block in the development of peptide-based drugs and bioactive molecules. The compound is often employed in asymmetric synthesis to introduce specific stereochemistry into target molecules, enhancing their biological activity or selectivity. Additionally, it is used in the preparation of proline derivatives, which are essential in designing enzyme inhibitors and receptor modulators. Its application extends to medicinal chemistry, where it aids in the creation of novel therapeutic agents targeting diseases such as cancer, viral infections, and neurological disorders. The allyl group in the structure also allows for further functionalization, making it a versatile intermediate in complex chemical transformations.
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