Fluorophenylethynylphenol, identified by its CAS number 197770-48-2, is an organic compound characterized by the presence of a phenol group substituted with both a fluorophenyl and an ethynyl group. This compound typically exhibits properties associated with both aromatic and alkyne functionalities, which can influence its reactivity and interactions. The fluorine atom in the fluorophenyl group can enhance the compound's lipophilicity and may also affect its electronic properties, making it potentially useful in various applications, including pharmaceuticals and materials science. The ethynyl group contributes to the compound's ability to participate in coupling reactions, which can be advantageous in synthetic chemistry. Additionally, the presence of the hydroxyl (-OH) group in the phenol structure can impart hydrogen bonding capabilities, influencing solubility and reactivity. Overall, Fluorophenylethynylphenol is a versatile compound with potential applications in diverse fields, including medicinal chemistry and organic synthesis.

Fluorophenylethynylphenol

197770-48-2: 4-(4-Fluorophenylethynyl)phenol

Phenol, 4-[2-(4-fluorophenyl)ethynyl]-

4-[(4-Fluorophenyl)ethynyl]phenol

4-(4-Fluorophenylethynyl)phenol

4-(4-Fluorophenylethynyl)phenol is a synthetic monomer that reacts with alkyne groups to form polymers. 4-(4-Fluorophenylethynyl)phenol is activated by the addition of azide and polymerized in the presence of triisopropylsilane. This technique can be used to synthesize acetylene-containing polymers, which are capable of absorbing infrared light. 4-(4-Fluorophenylethynyl)phenol has been shown to react with amides and polymers, forming amides and polymers containing functional groups.

CAS 197770-48-2: Fluorophenylethynylphenol

Phenol, 4-[2-(4-fluorophenyl)ethynyl]-

Ref: IN-DA002B0O

4-[(4-Fluorophenyl)ethynyl]phenol

Ref: 54-PC3963

4-(4-Fluorophenylethynyl)phenol

Ref: 3B-F0423

4-(4-Fluorophenylethynyl)phenol

Ref: 10-F009230

4-(4-Fluorophenylethynyl)phenol

Ref: 3D-FF61884