2-(2-Fluorophenyl)pyrimidine-5-carbaldehyde is an organic compound characterized by its pyrimidine core, which is a six-membered heterocyclic ring containing two nitrogen atoms at positions 1 and 3. The presence of a 2-fluorophenyl group indicates that a fluorine atom is substituted on the phenyl ring at the ortho position relative to the carbon that connects to the pyrimidine. The aldehyde functional group (-CHO) is located at the 5-position of the pyrimidine ring, contributing to its reactivity and potential applications in organic synthesis. This compound may exhibit properties such as moderate solubility in organic solvents and potential biological activity, making it of interest in medicinal chemistry. Its structure allows for various chemical modifications, which can be explored for developing new pharmaceuticals or agrochemicals. As with many heterocyclic compounds, it may also participate in various chemical reactions, including nucleophilic additions and condensation reactions, due to the electrophilic nature of the aldehyde group.

2-(2-fluorophenyl)pyrimidine-5-carbaldehyde

946707-17-1: 2-(2-Fluorophenyl)pyrimidine-5-carbaldehyde is an organic compound characterized by its pyrimidine core, which is a six-membered heterocyclic ring containing two nitrogen atoms at positions 1 and 3. The presence of a 2-fluorophenyl group indicates that a fluorine atom is substituted on the phenyl ring at the ortho position relative to the carbon that connects to the pyrimidine. The aldehyde functional group (-CHO) is located at the 5-position of the pyrimidine ring, contributing to its reactivity and potential applications in organic synthesis. This compound may exhibit properties such as moderate solubility in organic solvents and potential biological activity, making it of interest in medicinal chemistry. Its structure allows for various chemical modifications, which can be explored for developing new pharmaceuticals or agrochemicals. As with many heterocyclic compounds, it may also participate in various chemical reactions, including nucleophilic additions and condensation reactions, due to the electrophilic nature of the aldehyde group.

CAS 946707-17-1

2-(2-fluorophenyl)pyrimidine-5-carbaldehyde

2-(2-Fluorophenyl)pyrimidine-5-carbaldehyde

Ref: IN-DA006T7L

2-(2-Fluorophenyl)pyrimidine-5-carbaldehyde

Ref: 54-PC1005956

2-(2-Fluorophenyl)pyrimidine-5-carboxaldehye

Ref: 10-F078291