(1R,3S)-3-Amino-1-(Boc-amino)cyclopentane
95%
- Product Code: 69065
CAS:
774212-81-6
| Molecular Weight: | 200.28 g./mol | Molecular Formula: | C₁₀H₂₀N₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD18831392 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, dry |
Product Description:
This compound is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the development of peptidomimetics and other bioactive molecules. Its structure, featuring both amino and Boc-protected amino groups, makes it a valuable building block in organic chemistry for constructing complex cyclic peptides and small molecule inhibitors. It is often employed in drug discovery programs targeting various diseases, including cancer and neurological disorders, due to its ability to mimic peptide backbones and enhance drug stability. Additionally, it serves as a chiral scaffold in asymmetric synthesis, enabling the creation of enantiomerically pure compounds for therapeutic applications.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Colorless to brown or white to brown solid or liquid |
| PURITY | 95-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿5,445.00 |
+
-
|
| 0.250 | 10-20 days | ฿9,261.00 |
+
-
|
| 1.000 | 10-20 days | ฿22,626.00 |
+
-
|
(1R,3S)-3-Amino-1-(Boc-amino)cyclopentane
This compound is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the development of peptidomimetics and other bioactive molecules. Its structure, featuring both amino and Boc-protected amino groups, makes it a valuable building block in organic chemistry for constructing complex cyclic peptides and small molecule inhibitors. It is often employed in drug discovery programs targeting various diseases, including cancer and neurological disorders, due to its ability to mimic peptide backbones and enhance drug stability. Additionally, it serves as a chiral scaffold in asymmetric synthesis, enabling the creation of enantiomerically pure compounds for therapeutic applications.
| Mechanism | - |
| Appearance | - |
| Longevity | - |
| Strength | - |
| Storage | - |
| Shelf Life | - |
| Allergen(s) | - |
| Dosage (Range) | - |
| Recommended Dosage | - |
| Dosage (Per Day) | - |
| Recommended Dosage (Per Day) | - |
| Mix Method | - |
| Heat Resistance | - |
| Stable in pH range | - |
| Solubility | - |
| Product Types | - |
| INCI | - |
Cart
No products
Subtotal:
฿0.00
฿0.00
Total :