1-(2-(Trifluoromethyl)phenyl)-1H-pyrazole-4-carboxylic acid
98%
- Product Code: 114284
CAS:
1260855-51-3
| Molecular Weight: | 256.18 g./mol | Molecular Formula: | C₁₁H₇F₃N₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD15527664 | |
| Melting Point: | Boiling Point: | 382.9±42.0°C at 760 mmHg | |
| Density: | Storage Condition: | Room temperature, dry and sealed |
Product Description:
This compound is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various bioactive molecules, particularly those targeting specific enzymes or receptors. Its trifluoromethylphenyl group enhances binding affinity and metabolic stability, making it valuable in drug discovery. Additionally, it is explored in the synthesis of agrochemicals, where its structural features contribute to the efficacy of pesticides or herbicides. Its carboxylic acid functionality allows for further derivatization, enabling the creation of diverse chemical libraries for screening purposes.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | White To Off-White To Yellow Powder Or Crystals |
| Purity (%) | 97.5-100 |
| Infrared Spectrum | Conforms To Structure |
| NMR | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿2,290.00 |
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| 0.250 | 10-20 days | ฿4,590.00 |
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1-(2-(Trifluoromethyl)phenyl)-1H-pyrazole-4-carboxylic acid
This compound is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various bioactive molecules, particularly those targeting specific enzymes or receptors. Its trifluoromethylphenyl group enhances binding affinity and metabolic stability, making it valuable in drug discovery. Additionally, it is explored in the synthesis of agrochemicals, where its structural features contribute to the efficacy of pesticides or herbicides. Its carboxylic acid functionality allows for further derivatization, enabling the creation of diverse chemical libraries for screening purposes.
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