6-Bromo-3-(2-chloro-5-(trifluoromethyl)pyrimidin-4-yl)-1-(phenylsulfonyl)-1H-indole
98%
- Product Code: 49889
CAS:
2173193-44-5
| Molecular Weight: | 516.7188 g./mol | Molecular Formula: | C₁₉H₁₀BrClF₃N₃O₂S |
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| EC Number: | MDL Number: | MFCD32640880 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of biologically active compounds, particularly those targeting specific enzymes or receptors. Its structural features, including the indole core and pyrimidine moiety, make it valuable for developing potential drug candidates, especially in the areas of oncology and anti-inflammatory therapies. Researchers often employ it in the design and optimization of small molecules that can modulate protein interactions or inhibit critical pathways involved in disease progression. Additionally, its unique chemical structure allows for further functionalization, enabling the exploration of diverse pharmacological activities.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $206.69 |
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6-Bromo-3-(2-chloro-5-(trifluoromethyl)pyrimidin-4-yl)-1-(phenylsulfonyl)-1H-indole
This chemical is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of biologically active compounds, particularly those targeting specific enzymes or receptors. Its structural features, including the indole core and pyrimidine moiety, make it valuable for developing potential drug candidates, especially in the areas of oncology and anti-inflammatory therapies. Researchers often employ it in the design and optimization of small molecules that can modulate protein interactions or inhibit critical pathways involved in disease progression. Additionally, its unique chemical structure allows for further functionalization, enabling the exploration of diverse pharmacological activities.
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