AD43361
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
1g | 98% | in stock | $330.00 | $231.00 | - + | |
5g | 98% | in stock | $1,255.00 | $879.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AD43361 |
Chemical Name: | 4-Fluoro-3-phenylbenzoic acid |
CAS Number: | 1082484-37-4 |
Molecular Formula: | C13H9FO2 |
Molecular Weight: | 216.20776320000002 |
MDL Number: | MFCD11577106 |
SMILES: | OC(=O)c1ccc(c(c1)c1ccccc1)F |
4-Fluoro-3-phenylbenzoic acid, also known as $name$, serves as a versatile building block in chemical synthesis. This compound is commonly utilized as a key intermediate in the preparation of various pharmaceuticals, agrochemicals, and advanced materials. Its unique structure containing a fluoro group and a phenyl moiety imparts distinct reactivity and functionalization properties, making it a valuable component in organic synthesis strategies.One of the primary applications of 4-Fluoro-3-phenylbenzoic acid is in the synthesis of heterocyclic compounds. By reacting this compound with appropriate reagents or catalysts, chemists can access a diverse array of heterocycles such as benzothiazoles, benzoxazoles, and benzimidazoles. These heterocyclic motifs are prevalent in many bioactive molecules and have significant implications in medicinal chemistry and drug discovery.Furthermore, 4-Fluoro-3-phenylbenzoic acid can participate in transition-metal-catalyzed cross-coupling reactions, enabling the formation of C-C and C-heteroatom bonds. This capability allows for the construction of complex molecular architectures with precision and efficiency, facilitating the synthesis of novel compounds for various industrial applications.Additionally, the presence of the fluoro group in this compound introduces unique properties that can be harnessed in materials science. Fluorinated organic molecules are known for their tunable physicochemical characteristics, such as altered solubility, reactivity, and electronic properties. Therefore, by incorporating 4-Fluoro-3-phenylbenzoic acid into polymer synthesis or surface modification processes, researchers can tailor the properties of resulting materials for specific applications in coatings, adhesives, or electronic devices.