(S)-tert-Butyl 2-(5-(6-bromonaphthalen-2-yl)-1H-imidazol-2-yl)pyrrolidine-1-carboxylate
95%
- Product Code: 38152
CAS:
1228551-96-9
| Molecular Weight: | 442.3489 g./mol | Molecular Formula: | C₂₂H₂₄BrN₃O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD26392790 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in pharmaceutical research as a key intermediate in the synthesis of biologically active molecules. Its structure, featuring a bromonaphthalene group and an imidazole ring, makes it valuable in the development of potential drug candidates targeting specific enzymes or receptors. It is often employed in the design of inhibitors for therapeutic applications, particularly in areas such as oncology and inflammation. The compound’s chiral center also allows for the exploration of stereoselective interactions in drug development, enhancing the precision of pharmacological studies. Researchers leverage its unique properties to optimize drug efficacy and selectivity in preclinical studies.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿5,688.00 |
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(S)-tert-Butyl 2-(5-(6-bromonaphthalen-2-yl)-1H-imidazol-2-yl)pyrrolidine-1-carboxylate
This compound is primarily utilized in pharmaceutical research as a key intermediate in the synthesis of biologically active molecules. Its structure, featuring a bromonaphthalene group and an imidazole ring, makes it valuable in the development of potential drug candidates targeting specific enzymes or receptors. It is often employed in the design of inhibitors for therapeutic applications, particularly in areas such as oncology and inflammation. The compound’s chiral center also allows for the exploration of stereoselective interactions in drug development, enhancing the precision of pharmacological studies. Researchers leverage its unique properties to optimize drug efficacy and selectivity in preclinical studies.
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