Ethyl (1R,2S)-2-(Cbz-amino)cyclopentanecarboxylate
≥95%
- Product Code: 76132
CAS:
1140972-27-5
| Molecular Weight: | 291.34 g./mol | Molecular Formula: | C₁₆H₂₁NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD26404521 | |
| 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 and pharmaceuticals. It serves as a key intermediate in the synthesis of various biologically active compounds, including peptides and peptidomimetics. The presence of the Cbz (carbobenzyloxy) protecting group allows for selective deprotection during multi-step synthetic processes, ensuring the integrity of the amino group. Additionally, its cyclopentane ring structure contributes to the development of conformationally constrained analogs, which are valuable in drug discovery for enhancing potency and selectivity. The ethyl ester moiety further facilitates chemical modifications, making it a versatile building block in medicinal chemistry.
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 | ฿29,493.00 |
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| 1.000 | 10-20 days | ฿67,932.00 |
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Ethyl (1R,2S)-2-(Cbz-amino)cyclopentanecarboxylate
This compound is primarily used in organic synthesis, particularly in the preparation of complex molecules and pharmaceuticals. It serves as a key intermediate in the synthesis of various biologically active compounds, including peptides and peptidomimetics. The presence of the Cbz (carbobenzyloxy) protecting group allows for selective deprotection during multi-step synthetic processes, ensuring the integrity of the amino group. Additionally, its cyclopentane ring structure contributes to the development of conformationally constrained analogs, which are valuable in drug discovery for enhancing potency and selectivity. The ethyl ester moiety further facilitates chemical modifications, making it a versatile building block in medicinal chemistry.
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