1-Bromo-3-(trifluoromethyl)imidazo[1,5-a]pyridine-6-carboxylic acid
95%
- Product Code: 40013
CAS:
1781028-01-0
| Molecular Weight: | 309.0395 g./mol | Molecular Formula: | C₉H₄BrF₃N₂O₂ |
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| EC Number: | MDL Number: | MFCD28595110 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active molecules. Its structure, featuring both a trifluoromethyl group and a carboxylic acid moiety, makes it a versatile building block for designing pharmaceutical agents. It is often employed in the development of potential drug candidates targeting various diseases, including cancer and infectious diseases. The trifluoromethyl group enhances the metabolic stability and bioavailability of the resulting compounds, while the carboxylic acid allows for further functionalization or interaction with biological targets. Additionally, its imidazo[1,5-a]pyridine core is valuable in creating compounds with potential therapeutic effects due to its ability to mimic natural heterocycles found in bioactive molecules.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿5,607.00 |
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1-Bromo-3-(trifluoromethyl)imidazo[1,5-a]pyridine-6-carboxylic acid
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active molecules. Its structure, featuring both a trifluoromethyl group and a carboxylic acid moiety, makes it a versatile building block for designing pharmaceutical agents. It is often employed in the development of potential drug candidates targeting various diseases, including cancer and infectious diseases. The trifluoromethyl group enhances the metabolic stability and bioavailability of the resulting compounds, while the carboxylic acid allows for further functionalization or interaction with biological targets. Additionally, its imidazo[1,5-a]pyridine core is valuable in creating compounds with potential therapeutic effects due to its ability to mimic natural heterocycles found in bioactive molecules.
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