tert-Butyl 2-(5-bromo-1H-imidazol-2-yl)pyrrolidine-1-carboxylate
97%
- Product Code: 41770
CAS:
1352718-88-7
| Molecular Weight: | 316.1942 g./mol | Molecular Formula: | C₁₂H₁₈BrN₃O₂ |
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| EC Number: | MDL Number: | MFCD24467648 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized in organic synthesis as a key intermediate in the development of pharmaceutical compounds. Its structure, featuring both imidazole and pyrrolidine rings, makes it valuable for constructing biologically active molecules, particularly in drug discovery and medicinal chemistry. It is often employed in the synthesis of inhibitors or modulators targeting enzymes or receptors, especially in the field of oncology and neurology. The bromo group on the imidazole ring allows for further functionalization through cross-coupling reactions, enabling the creation of diverse derivatives for biological evaluation. Additionally, the tert-butyloxycarbonyl (Boc) protecting group enhances its stability during synthetic processes, making it a practical choice for multi-step organic transformations.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿2,745.00 |
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tert-Butyl 2-(5-bromo-1H-imidazol-2-yl)pyrrolidine-1-carboxylate
This chemical is primarily utilized in organic synthesis as a key intermediate in the development of pharmaceutical compounds. Its structure, featuring both imidazole and pyrrolidine rings, makes it valuable for constructing biologically active molecules, particularly in drug discovery and medicinal chemistry. It is often employed in the synthesis of inhibitors or modulators targeting enzymes or receptors, especially in the field of oncology and neurology. The bromo group on the imidazole ring allows for further functionalization through cross-coupling reactions, enabling the creation of diverse derivatives for biological evaluation. Additionally, the tert-butyloxycarbonyl (Boc) protecting group enhances its stability during synthetic processes, making it a practical choice for multi-step organic transformations.
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