CAS 3798-61-6
:Benzenemethanol, a-ethynyl-4-fluoro-
Description:
Benzenemethanol, α-ethynyl-4-fluoro- (CAS 3798-61-6) is an organic compound characterized by its structure, which includes a benzene ring substituted with a hydroxymethyl group and an ethynyl group, along with a fluorine atom at the para position relative to the hydroxymethyl group. This compound is typically a colorless to pale yellow liquid or solid, depending on its purity and specific conditions. It exhibits properties common to aromatic compounds, such as stability and the ability to participate in electrophilic substitution reactions. The presence of the ethynyl group introduces a triple bond, which can engage in various chemical reactions, including polymerization and coupling reactions. The fluorine atom enhances the compound's reactivity and can influence its physical properties, such as solubility and boiling point. Benzenemethanol derivatives are often studied for their potential applications in pharmaceuticals, agrochemicals, and materials science due to their unique chemical properties and functional groups.
Formula:C9H7FO
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Found 3 products.
1-(4-Fluorophenyl)-2-propyn-1-ol
CAS:<p>1-Phenyl-2-propen-1-ol is a carbene that has been synthesized by the reaction of 1,4-difluorobenzene and resorcinol in the presence of copper. The compound has two skeletal isomers, cis and trans. The equilibrium constant for the reaction is K=3.5×10^(-8) at 25°C. It can be used as a ligand to form ruthenium complexes with electrophilic metals such as chlorine or bromine. The x-ray crystal structure for cis isomer has been determined and it was found to have an intramolecular bond from the hydrogen atom on the phenyl group to the carbon atom on the propynyl group. This bond causes resonance stabilization of this molecule in its ground state. Carbocationic reactions are also possible with this molecule, but they are not normally observed because of steric hindrance from substituents on both rings</p>Formula:C9H7FOPurity:Min. 95%Molecular weight:150.15 g/mol


