[(2-Fluorophenyl)sulfanyl]acetate, with the CAS number 705-02-2, is an organic compound characterized by the presence of a fluorinated aromatic ring and a thioether functional group. The molecule features a 2-fluorophenyl group, which indicates that a fluorine atom is substituted at the second position of the phenyl ring, enhancing its reactivity and influencing its physical properties. The sulfanyl (thioether) group contributes to the compound's potential as a nucleophile in various chemical reactions. The acetate moiety suggests that the compound can participate in esterification and hydrolysis reactions. In terms of physical properties, compounds like this often exhibit moderate solubility in organic solvents and may have distinct melting and boiling points influenced by the presence of the fluorine atom and the overall molecular structure. The compound's unique characteristics make it of interest in fields such as medicinal chemistry and materials science, where fluorinated compounds are often explored for their enhanced biological activity and stability.

[(2-fluorophenyl)sulfanyl]acetate

705-02-2: [(2-Fluorophenyl)sulfanyl]acetate, with the CAS number 705-02-2, is an organic compound characterized by the presence of a fluorinated aromatic ring and a thioether functional group. The molecule features a 2-fluorophenyl group, which indicates that a fluorine atom is substituted at the second position of the phenyl ring, enhancing its reactivity and influencing its physical properties. The sulfanyl (thioether) group contributes to the compound's potential as a nucleophile in various chemical reactions. The acetate moiety suggests that the compound can participate in esterification and hydrolysis reactions. In terms of physical properties, compounds like this often exhibit moderate solubility in organic solvents and may have distinct melting and boiling points influenced by the presence of the fluorine atom and the overall molecular structure. The compound's unique characteristics make it of interest in fields such as medicinal chemistry and materials science, where fluorinated compounds are often explored for their enhanced biological activity and stability.

<p>Applications 2-[(2-fluorophenyl)sulfanyl]acetic acid (cas# 705-02-2) is used in the preparation of phenylsulfanylalkylcarboxylic acid compositions, useful for the delivery of active agents.<br>References Wang, N. F., et al.: PCT Int. Appl. 118 pp. (2008)<br></p>

CAS 705-02-2

[(2-fluorophenyl)sulfanyl]acetate

2-[(2-Fluorophenyl)sulfanyl]acetic Acid

Ref: TR-F589910