2-Fluoro-5-(4-trifluoromethylphenyl)benzoic acid
≥95%
- Product Code: 86714
CAS:
1179671-81-8
Molecular Weight: | 284.21 g./mol | Molecular Formula: | C₁₄H₈F₄O₂ |
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EC Number: | MDL Number: | MFCD18321790 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | 2-8°C, dry, airtight |
Product Description:
This chemical is primarily utilized in the field of organic synthesis, particularly as an intermediate in the production of pharmaceuticals and agrochemicals. Its structure, featuring both fluorine and trifluoromethyl groups, makes it valuable in the development of compounds with enhanced biological activity and stability. It is often employed in the synthesis of active pharmaceutical ingredients (APIs) where the introduction of fluorine atoms can improve metabolic stability and bioavailability. Additionally, it serves as a building block in the creation of advanced materials, including liquid crystals and polymers, due to its unique electronic properties. Its application in medicinal chemistry is notable for designing drugs targeting specific receptors or enzymes, leveraging its ability to modulate molecular interactions.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.250 | 10-20 days | $129.54 |
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2-Fluoro-5-(4-trifluoromethylphenyl)benzoic acid
This chemical is primarily utilized in the field of organic synthesis, particularly as an intermediate in the production of pharmaceuticals and agrochemicals. Its structure, featuring both fluorine and trifluoromethyl groups, makes it valuable in the development of compounds with enhanced biological activity and stability. It is often employed in the synthesis of active pharmaceutical ingredients (APIs) where the introduction of fluorine atoms can improve metabolic stability and bioavailability. Additionally, it serves as a building block in the creation of advanced materials, including liquid crystals and polymers, due to its unique electronic properties. Its application in medicinal chemistry is notable for designing drugs targeting specific receptors or enzymes, leveraging its ability to modulate molecular interactions.
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