(2S)-Dicyclohexylamine trans-1-(tert-butoxycarbonyl)-4-hydroxypyrrolidine-2-carboxylate
97%
- Product Code: 52567
CAS:
21157-12-0
| Molecular Weight: | 412.5700 g./mol | Molecular Formula: | C₂₂H₄₀N₂O₅ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00076980 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized in the pharmaceutical industry as an intermediate in the synthesis of complex organic compounds. Its structure, featuring a protected amine and hydroxyl group, makes it valuable in the development of peptide-based drugs and other bioactive molecules. The tert-butoxycarbonyl (Boc) group provides stability during chemical reactions, allowing for selective deprotection when needed. It is often employed in the preparation of chiral compounds, particularly in the synthesis of enantiomerically pure substances, which are critical in the production of medications with specific therapeutic effects. Additionally, its pyrrolidine ring structure is commonly found in molecules targeting neurological and cardiovascular diseases, making it a key component in drug discovery and development processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | €12.35 |
+
-
|
(2S)-Dicyclohexylamine trans-1-(tert-butoxycarbonyl)-4-hydroxypyrrolidine-2-carboxylate
This chemical is primarily utilized in the pharmaceutical industry as an intermediate in the synthesis of complex organic compounds. Its structure, featuring a protected amine and hydroxyl group, makes it valuable in the development of peptide-based drugs and other bioactive molecules. The tert-butoxycarbonyl (Boc) group provides stability during chemical reactions, allowing for selective deprotection when needed. It is often employed in the preparation of chiral compounds, particularly in the synthesis of enantiomerically pure substances, which are critical in the production of medications with specific therapeutic effects. Additionally, its pyrrolidine ring structure is commonly found in molecules targeting neurological and cardiovascular diseases, making it a key component in drug discovery and development processes.
| 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 :