2-(Trifluoromethyl)-1H-imidazole-5-carboxylic acid
96%
- Product Code: 79115
CAS:
78016-98-5
| Molecular Weight: | 180.08 g./mol | Molecular Formula: | C₅H₃F₃N₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD10696306 | |
| Melting Point: | Boiling Point: | 350.7°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This chemical is primarily utilized in pharmaceutical research and development, particularly in the synthesis of bioactive compounds. Its trifluoromethyl group enhances the metabolic stability and bioavailability of drug candidates, making it valuable in designing molecules with improved therapeutic properties. It is often employed as a building block in the creation of small-molecule inhibitors targeting enzymes or receptors involved in various diseases. Additionally, its imidazole core structure is useful in developing compounds with potential antifungal, antibacterial, or anti-inflammatory activities. The carboxylic acid group allows for further chemical modifications, enabling the creation of diverse derivatives for structure-activity relationship studies. Its applications extend to agrochemical research, where it contributes to the development of novel pesticides or herbicides with enhanced efficacy.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | ฿16,800.00 |
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| 0.250 | 10-20 days | ฿42,980.00 |
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2-(Trifluoromethyl)-1H-imidazole-5-carboxylic acid
This chemical is primarily utilized in pharmaceutical research and development, particularly in the synthesis of bioactive compounds. Its trifluoromethyl group enhances the metabolic stability and bioavailability of drug candidates, making it valuable in designing molecules with improved therapeutic properties. It is often employed as a building block in the creation of small-molecule inhibitors targeting enzymes or receptors involved in various diseases. Additionally, its imidazole core structure is useful in developing compounds with potential antifungal, antibacterial, or anti-inflammatory activities. The carboxylic acid group allows for further chemical modifications, enabling the creation of diverse derivatives for structure-activity relationship studies. Its applications extend to agrochemical research, where it contributes to the development of novel pesticides or herbicides with enhanced efficacy.
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