N-(3-Trifluoromethylphenyl)anthranilic Acid
≥98%
- Product Code: 99144
CAS:
530-78-9
| Molecular Weight: | 281.23 g./mol | Molecular Formula: | C₁₄H₁₀F₃NO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00002422 | |
| Melting Point: | 133-137°C | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized in the synthesis of pharmaceutical compounds, particularly nonsteroidal anti-inflammatory drugs (NSAIDs). Its structure allows it to act as a key intermediate in the production of medications that target inflammation and pain relief. Additionally, it is employed in research and development for creating novel therapeutic agents due to its trifluoromethyl group, which enhances the biological activity and stability of the resulting compounds. Its applications also extend to the field of organic chemistry, where it serves as a building block for complex molecules in various synthetic pathways.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Off white powder |
| PURITY | 98 100% |
| MELTING POINT | 133-137 |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | Ft3,124.49 |
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| 5.000 | 10-20 days | Ft10,127.66 |
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| 25.000 | 10-20 days | Ft24,457.23 |
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| 100.000 | 10-20 days | Ft75,418.76 |
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| 500.000 | 10-20 days | Ft298,766.01 |
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N-(3-Trifluoromethylphenyl)anthranilic Acid
This chemical is primarily utilized in the synthesis of pharmaceutical compounds, particularly nonsteroidal anti-inflammatory drugs (NSAIDs). Its structure allows it to act as a key intermediate in the production of medications that target inflammation and pain relief. Additionally, it is employed in research and development for creating novel therapeutic agents due to its trifluoromethyl group, which enhances the biological activity and stability of the resulting compounds. Its applications also extend to the field of organic chemistry, where it serves as a building block for complex molecules in various synthetic pathways.
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