2-(4-Chlorophenyl)pyridine, also known by its CAS number 5969-83-5, is an organic compound characterized by a pyridine ring substituted with a 4-chlorophenyl group. This compound typically appears as a colorless to pale yellow liquid or solid, depending on its purity and form. It has a molecular formula that reflects its aromatic nature, contributing to its stability and reactivity. The presence of the chlorophenyl group enhances its lipophilicity, making it soluble in organic solvents while exhibiting limited solubility in water. This compound is of interest in various fields, including pharmaceuticals and agrochemicals, due to its potential biological activity. Its structure allows for interactions with biological targets, which can lead to applications in drug development. Additionally, 2-(4-Chlorophenyl)pyridine may undergo typical reactions associated with aromatic compounds, such as electrophilic substitution. Safety data should be consulted for handling, as it may pose health risks if not managed properly. Overall, this compound exemplifies the diverse chemistry of substituted pyridines.

2-(4-Chlorophenyl)pyridine

2-(4-Chlorophenyl)pyridine is a synthetic molecule that has been shown to have significant antiproliferative activity in cancer cells. This compound has been immobilized on silica gel and has been used as a catalyst for cross-coupling reactions. It can be used to synthesize phenylpyridines, amines, and other molecules with high selectivity. 2-(4-Chlorophenyl)pyridine has also been found to be an effective surrogate for the study of DNA photoproducts formed by irradiation of DNA with ultraviolet light or ionizing radiation.

CAS 5969-83-5: 2-(4-Chlorophenyl)pyridine

2-(4-Chlorophenyl)pyridine

Ref: 3D-FC63147

Vismodegib Impurity 14

Ref: ST-EA-CP-V25012

2-(4-chlorophenyl)pyridine

Ref: IN-DA00E97D

2-(4-Chlorophenyl)pyridine

Ref: 10-F022560

2-(4-Chlorophenyl)pyridine

Ref: 54-OR962436

2-(4-Chlorophenyl)pyridine

Ref: 3B-C3764