CAS 73322-01-7

Pyridine, 2-[(4-nitrophenyl)thio]-

Description:

Pyridine, 2-[(4-nitrophenyl)thio]- is an organic compound characterized by a pyridine ring substituted with a 4-nitrophenylthio group. The presence of the pyridine moiety imparts basic properties to the compound, making it a weak base. The 4-nitrophenylthio group introduces both electron-withdrawing characteristics due to the nitro group and a sulfur atom that can participate in various chemical reactions, such as nucleophilic substitutions or redox reactions. This compound is typically used in organic synthesis and may serve as an intermediate in the production of pharmaceuticals, agrochemicals, or dyes. Its solubility in organic solvents and moderate stability under standard conditions make it suitable for various applications in chemical research. However, like many nitro compounds, it may pose environmental and health risks, necessitating careful handling and disposal. Overall, Pyridine, 2-[(4-nitrophenyl)thio]- exemplifies the complexity and utility of substituted pyridines in synthetic organic chemistry.

Formula: C₁₁H₈N₂O₂S

2-[(4-Nitrophenyl)sulfanyl]pyridine

CAS: 73322-01-7

2-[(4-Nitrophenyl)sulfanyl]pyridine

Purity: ≥95%

Molecular weight: 232.26g/mol

Ref: 54-OR311063

1-Nitro-4-(2-pyridylthio)benzene

CAS: 73322-01-7

Formula: C₁₁H₈N₂O₂S

Purity: 95.0%

Color and Shape: Solid

Molecular weight: 232.26

Ref: 10-F068398

1-Nitro-4-(2-pyridylthio)benzene

CAS: 73322-01-7

1-Nitro-4-(2-pyridylthio)benzene is a crystalline solid that can be found in the form of its selenoxide. It has been shown to have catalytic activity and is used as a precursor for the synthesis of heterocycles. 1-Nitro-4-(2-pyridylthio)benzene has also been employed in studies on the coordination chemistry of piperidine and phenylacetylene. This selenoxide has also been shown to have antiinflammatory properties, which may be due to its ability to inhibit prostaglandin synthesis.

Purity: Min. 95%

Ref: 3D-FN168959