(R)-tert-Butyl (1-(5-bromopyridin-2-yl)-2-hydroxyethyl)carbamate
97%
- Product Code: 37272
CAS:
2126088-15-9
| Molecular Weight: | 317.18 g./mol | Molecular Formula: | C₁₂H₁₇BrN₂O₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD31539627 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, dry and sealed |
Product Description:
This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of chiral intermediates for drug candidates. Its structure, featuring a bromopyridine moiety and a protected amino alcohol group, makes it a valuable building block in the creation of biologically active molecules. It is often employed in the preparation of compounds targeting central nervous system disorders, inflammation, and other therapeutic areas. The chiral center allows for the development of enantiomerically pure drugs, which is crucial for optimizing efficacy and reducing side effects. Additionally, its bromine atom serves as a reactive site for further functionalization through cross-coupling reactions, enabling the construction of more complex molecular architectures.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $420.97 |
+
-
|
| 0.250 | 10-20 days | $841.94 |
+
-
|
(R)-tert-Butyl (1-(5-bromopyridin-2-yl)-2-hydroxyethyl)carbamate
This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of chiral intermediates for drug candidates. Its structure, featuring a bromopyridine moiety and a protected amino alcohol group, makes it a valuable building block in the creation of biologically active molecules. It is often employed in the preparation of compounds targeting central nervous system disorders, inflammation, and other therapeutic areas. The chiral center allows for the development of enantiomerically pure drugs, which is crucial for optimizing efficacy and reducing side effects. Additionally, its bromine atom serves as a reactive site for further functionalization through cross-coupling reactions, enabling the construction of more complex molecular architectures.
| 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 :