(S)-tert-Butyl 2-(6-bromo-1H-benzo[d]imidazol-2-yl)pyrrolidine-1-carboxylate
97%
- Product Code: 113713
CAS:
1208007-67-3
| Molecular Weight: | 366.25 g./mol | Molecular Formula: | C₁₆H₂₀BrN₃O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD22418840 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This chemical is primarily utilized in the pharmaceutical and biotechnology industries as a key intermediate in the synthesis of complex organic compounds. Its structure, featuring a bromo-substituted benzimidazole ring and a pyrrolidine moiety, makes it a valuable building block for developing biologically active molecules. It is often employed in the preparation of potential drug candidates, particularly those targeting enzyme inhibition or receptor modulation. The presence of the bromo group allows for further functionalization through cross-coupling reactions, enabling the creation of diverse derivatives for medicinal chemistry research. Additionally, its chiral nature makes it useful in the development of enantioselective compounds, which are critical in designing drugs with improved efficacy and reduced side effects.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿666.00 |
+
-
|
| 1.000 | 10-20 days | ฿1,791.00 |
+
-
|
| 5.000 | 10-20 days | ฿6,264.00 |
+
-
|
(S)-tert-Butyl 2-(6-bromo-1H-benzo[d]imidazol-2-yl)pyrrolidine-1-carboxylate
This chemical is primarily utilized in the pharmaceutical and biotechnology industries as a key intermediate in the synthesis of complex organic compounds. Its structure, featuring a bromo-substituted benzimidazole ring and a pyrrolidine moiety, makes it a valuable building block for developing biologically active molecules. It is often employed in the preparation of potential drug candidates, particularly those targeting enzyme inhibition or receptor modulation. The presence of the bromo group allows for further functionalization through cross-coupling reactions, enabling the creation of diverse derivatives for medicinal chemistry research. Additionally, its chiral nature makes it useful in the development of enantioselective compounds, which are critical in designing drugs with improved efficacy and reduced side effects.
| 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 :