3-Trifluoromethyl-4'-methoxydiphenylamine
≥95%
- Product Code: 66449
CAS:
1494-26-4
| Molecular Weight: | 267.25 g./mol | Molecular Formula: | C₁₄H₁₂F₃NO |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00143198 | |
| Melting Point: | 56-61°C | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily used in the synthesis of advanced materials and organic compounds, particularly in the development of liquid crystals for display technologies. Its unique structure allows it to contribute to the stability and performance of these materials, making it valuable in the production of high-quality screens for devices like smartphones, monitors, and televisions. Additionally, it serves as an intermediate in the manufacture of pharmaceuticals, where it plays a role in creating compounds with potential therapeutic applications. Its trifluoromethyl group enhances the chemical's reactivity and selectivity, making it a useful component in various organic reactions.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to Almost white powder to crystal |
| PURITY | 95-100 |
| MELTING POINT C | 56.0-61.0 |
| Infrared spectrum | Conforms to Structure |
| SOLUBILITY IN METHANOL | almost transparency |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.200 | 10-20 days | $130.82 |
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| 1.000 | 10-20 days | $431.90 |
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3-Trifluoromethyl-4'-methoxydiphenylamine
This chemical is primarily used in the synthesis of advanced materials and organic compounds, particularly in the development of liquid crystals for display technologies. Its unique structure allows it to contribute to the stability and performance of these materials, making it valuable in the production of high-quality screens for devices like smartphones, monitors, and televisions. Additionally, it serves as an intermediate in the manufacture of pharmaceuticals, where it plays a role in creating compounds with potential therapeutic applications. Its trifluoromethyl group enhances the chemical's reactivity and selectivity, making it a useful component in various organic reactions.
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