4-Bromo-1H-benzo[d]imidazol-2-amine
97%
- Product Code: 119262
CAS:
1266114-75-3
| Molecular Weight: | 212.05 g./mol | Molecular Formula: | C₇H₆BrN₃ |
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| EC Number: | MDL Number: | MFCD09907621 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, away from light, stored in an inert gas |
Product Description:
4-Bromo-1H-benzo[d]imidazol-2-amine is primarily used in the synthesis of various pharmaceutical compounds. It serves as a key intermediate in the development of drugs targeting specific biological pathways. The compound is particularly valuable in the creation of molecules with potential anti-cancer, anti-inflammatory, and anti-microbial properties. Its structure allows for further chemical modifications, making it versatile in medicinal chemistry research. Additionally, it is utilized in the study of enzyme inhibition and receptor binding, aiding in the discovery of new therapeutic agents. The bromo group attached to the benzimidazole ring enhances its reactivity, facilitating its use in cross-coupling reactions and other organic transformations essential for drug development.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿2,646.00 |
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| 1.000 | 10-20 days | ฿6,660.00 |
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| 5.000 | 10-20 days | ฿23,967.00 |
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| 10.000 | 10-20 days | ฿43,101.00 |
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4-Bromo-1H-benzo[d]imidazol-2-amine
4-Bromo-1H-benzo[d]imidazol-2-amine is primarily used in the synthesis of various pharmaceutical compounds. It serves as a key intermediate in the development of drugs targeting specific biological pathways. The compound is particularly valuable in the creation of molecules with potential anti-cancer, anti-inflammatory, and anti-microbial properties. Its structure allows for further chemical modifications, making it versatile in medicinal chemistry research. Additionally, it is utilized in the study of enzyme inhibition and receptor binding, aiding in the discovery of new therapeutic agents. The bromo group attached to the benzimidazole ring enhances its reactivity, facilitating its use in cross-coupling reactions and other organic transformations essential for drug development.
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