AB62108
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
1g | 98% | in stock | $6.00 | $5.00 | - + | |
5g | 98% | in stock | $12.00 | $9.00 | - + | |
10g | 98% | in stock | $23.00 | $17.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AB62108 |
Chemical Name: | 2-Fluoro-3-(trifluoromethyl)benzaldehyde |
CAS Number: | 112641-20-0 |
Molecular Formula: | C8H4F4O |
Molecular Weight: | 192.1104 |
MDL Number: | MFCD00061246 |
SMILES: | O=Cc1cccc(c1F)C(F)(F)F |
Complexity: | 189 |
Covalently-Bonded Unit Count: | 1 |
Heavy Atom Count: | 13 |
Hydrogen Bond Acceptor Count: | 5 |
Rotatable Bond Count: | 1 |
XLogP3: | 2.4 |
2-Fluoro-3-(trifluoromethyl)benzaldehyde is a versatile compound widely used in chemical synthesis due to its unique properties and reactivity. This fluorinated benzaldehyde serves as a key building block in the preparation of various pharmaceuticals, agrochemicals, and specialty chemicals. Its distinctive structure, combining a fluoro group with a trifluoromethyl group, imparts valuable characteristics that are crucial for designing and synthesizing complex molecules with specific biological or physical properties.In chemical synthesis, 2-Fluoro-3-(trifluoromethyl)benzaldehyde acts as a valuable intermediate for the introduction of fluorine and trifluoromethyl groups into organic molecules. These functional groups are highly sought after in medicinal chemistry and materials science due to their beneficial effects on molecular stability, lipophilicity, and biological activity. The presence of a fluorine atom enhances the metabolic stability and binding affinities of drug candidates, making fluorinated compounds promising candidates for drug discovery and development.Moreover, the trifluoromethyl group confers unique physicochemical properties that can influence the solubility, lipophilicity, and reactivity of the resulting molecules. This can lead to improved pharmacokinetic profiles, increased bioavailability, and enhanced biological interactions, making 2-Fluoro-3-(trifluoromethyl)benzaldehyde an invaluable tool for accessing structurally diverse compounds with tailored properties.Overall, the strategic incorporation of 2-Fluoro-3-(trifluoromethyl)benzaldehyde in chemical synthesis enables researchers to access a wide range of fluorinated and trifluoromethylated compounds with potential applications in drug development, materials science, and other fields that demand precision and innovation in molecular design.