(3-Nitro-5-trifluoromethyl-phenyl)-methanol
95%
- Product Code: 57321
CAS:
180146-66-1
| Molecular Weight: | 221.13 g./mol | Molecular Formula: | C₈H₆F₃NO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD11040241 | |
| Melting Point: | Boiling Point: | 281.2±35.0 °C(Predicted) | |
| Density: | 1.488±0.06 g/cm3(Predicted) | Storage Condition: | room temperature |
Product Description:
(3-Nitro-5-trifluoromethyl-phenyl)-methanol finds its primary application in organic synthesis, where it serves as an intermediate in the production of more complex chemical compounds. Its structure, featuring both a nitro group and a trifluoromethyl group, makes it a valuable building block for pharmaceuticals and agrochemicals. The nitro group can be reduced to an amine, enabling further functionalization, while the trifluoromethyl group enhances the stability and bioavailability of the resulting molecules. This compound is particularly useful in the development of active pharmaceutical ingredients (APIs) and specialty chemicals, where its unique properties contribute to the creation of compounds with specific biological or chemical activities.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | $35.64 |
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| 0.250 | 10-20 days | $75.61 |
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| 1.000 | 10-20 days | $234.92 |
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(3-Nitro-5-trifluoromethyl-phenyl)-methanol
(3-Nitro-5-trifluoromethyl-phenyl)-methanol finds its primary application in organic synthesis, where it serves as an intermediate in the production of more complex chemical compounds. Its structure, featuring both a nitro group and a trifluoromethyl group, makes it a valuable building block for pharmaceuticals and agrochemicals. The nitro group can be reduced to an amine, enabling further functionalization, while the trifluoromethyl group enhances the stability and bioavailability of the resulting molecules. This compound is particularly useful in the development of active pharmaceutical ingredients (APIs) and specialty chemicals, where its unique properties contribute to the creation of compounds with specific biological or chemical activities.
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