Ethyl (1S,2R)-2-(Cbz-amino)cyclopentanecarboxylate
≥95%
- Product Code: 76143
CAS:
1140972-32-2
| Molecular Weight: | 291.34 g./mol | Molecular Formula: | C₁₆H₂₁NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD26404522 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, dry |
Product Description:
This compound is primarily used in organic synthesis, particularly in the preparation of complex molecules. It serves as a key intermediate in the production of pharmaceuticals, especially in the synthesis of peptide-based drugs and other bioactive compounds. Its structure, featuring a cyclopentane ring and a Cbz-protected amino group, makes it valuable for constructing chiral molecules, which are crucial in medicinal chemistry. Additionally, it is employed in research and development for creating novel compounds with potential therapeutic applications. Its versatility in chemical reactions, such as coupling and cyclization, further enhances its utility in drug discovery and development processes.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Colorless to yellow liquid |
| PURITY | 95-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿42,300.00 |
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| 1.000 | 10-20 days | ฿122,580.00 |
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Ethyl (1S,2R)-2-(Cbz-amino)cyclopentanecarboxylate
This compound is primarily used in organic synthesis, particularly in the preparation of complex molecules. It serves as a key intermediate in the production of pharmaceuticals, especially in the synthesis of peptide-based drugs and other bioactive compounds. Its structure, featuring a cyclopentane ring and a Cbz-protected amino group, makes it valuable for constructing chiral molecules, which are crucial in medicinal chemistry. Additionally, it is employed in research and development for creating novel compounds with potential therapeutic applications. Its versatility in chemical reactions, such as coupling and cyclization, further enhances its utility in drug discovery and development processes.
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