2-(4-Bromophenyl)-1H-imidazo[4,5-c]pyridine
≥95%
- Product Code: 115763
CAS:
113270-73-8
| Molecular Weight: | 274.12 g./mol | Molecular Formula: | C₁₂H₈BrN₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD06657714 | |
| Melting Point: | Boiling Point: | 465.6°C at 760 mmHg | |
| Density: | Storage Condition: | Room temperature, dry and sealed |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry, where it serves as a key intermediate in the synthesis of various biologically active molecules. Its structure is particularly valuable in the development of pharmaceutical agents targeting specific diseases, such as cancer and inflammatory disorders. Researchers leverage its imidazopyridine core to design and optimize drug candidates with enhanced efficacy and selectivity. Additionally, it is employed in the study of enzyme inhibition and receptor binding, contributing to the discovery of novel therapeutic pathways. Its bromophenyl group further allows for functionalization, enabling the creation of diverse derivatives for structure-activity relationship studies.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿1,836.00 |
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| 0.250 | 10-20 days | ฿2,466.00 |
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2-(4-Bromophenyl)-1H-imidazo[4,5-c]pyridine
This compound is primarily utilized in the field of medicinal chemistry, where it serves as a key intermediate in the synthesis of various biologically active molecules. Its structure is particularly valuable in the development of pharmaceutical agents targeting specific diseases, such as cancer and inflammatory disorders. Researchers leverage its imidazopyridine core to design and optimize drug candidates with enhanced efficacy and selectivity. Additionally, it is employed in the study of enzyme inhibition and receptor binding, contributing to the discovery of novel therapeutic pathways. Its bromophenyl group further allows for functionalization, enabling the creation of diverse derivatives for structure-activity relationship studies.
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