2-Nitro-5-(trifluoromethyl)phenol
95%
- Product Code: 79300
CAS:
402-17-5
Molecular Weight: | 207.11 g./mol | Molecular Formula: | C₇H₄F₃NO₃ |
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EC Number: | MDL Number: | MFCD08282785 | |
Melting Point: | Boiling Point: | 239.355°C at 760 mmHg | |
Density: | Storage Condition: | room temperature, stored under inert gas |
Product Description:
2-Nitro-5-(trifluoromethyl)phenol is primarily used in organic synthesis as an intermediate for the production of more complex chemical compounds. Its unique structure, featuring both nitro and trifluoromethyl groups, makes it valuable in the development of pharmaceuticals, agrochemicals, and specialty chemicals. In pharmaceutical research, it serves as a building block for creating molecules with potential therapeutic properties, particularly in the design of drugs targeting specific enzymes or receptors. In agrochemical applications, it is utilized in the synthesis of herbicides and pesticides, where its electron-withdrawing groups enhance the activity and stability of the final product. Additionally, it finds use in material science for the development of advanced polymers and coatings, leveraging its chemical reactivity to improve material properties.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.250 | 10-20 days | €43.93 |
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1.000 | 10-20 days | €74.79 |
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5.000 | 10-20 days | €222.00 |
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10.000 | 10-20 days | €442.82 |
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2-Nitro-5-(trifluoromethyl)phenol
2-Nitro-5-(trifluoromethyl)phenol is primarily used in organic synthesis as an intermediate for the production of more complex chemical compounds. Its unique structure, featuring both nitro and trifluoromethyl groups, makes it valuable in the development of pharmaceuticals, agrochemicals, and specialty chemicals. In pharmaceutical research, it serves as a building block for creating molecules with potential therapeutic properties, particularly in the design of drugs targeting specific enzymes or receptors. In agrochemical applications, it is utilized in the synthesis of herbicides and pesticides, where its electron-withdrawing groups enhance the activity and stability of the final product. Additionally, it finds use in material science for the development of advanced polymers and coatings, leveraging its chemical reactivity to improve material properties.
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