Name | 2-(4-Nitrophenyl)pyridine |
Synonyms | 5-NITRO-2-PHENYLPYRIDINE 3-Nitro-6-phenylpyridine 5-nitro-2-phenylpyridine 2-PHENYL-5-NITROPYRIDINE 2-(p-Nitrophenyl)pyridine 2-(4-NITROPHENYL)PYRIDINE 2-(4-Nitrophenyl)pyridine Pyridine, 2-(4-nitrophenyl)- pyridine, 2-(4-nitrophenyl)- |
CAS | 4282-47-7 |
InChI | InChI=1/C11H8N2O2/c14-13(15)10-6-7-11(12-8-10)9-4-2-1-3-5-9/h1-8H |
InChIKey | FNLTWLXKZQWUJZ-UHFFFAOYSA-N |
Molecular Formula | C11H8N2O2 |
Molar Mass | 200.19 |
Density | 1.252±0.06 g/cm3(Predicted) |
Melting Point | 116-118 |
Boling Point | 354.3±17.0 °C(Predicted) |
Flash Point | 161.9°C |
Vapor Presure | 0.000134mmHg at 25°C |
pKa | 3.66±0.25(Predicted) |
Storage Condition | Keep in dark place,Sealed in dry,Room Temperature |
Refractive Index | 1.611 |
Hazard Symbols | Xi - Irritant |
Hazard Note | Irritant |
Overview | In the field of organic chemistry, pyridine structure modules are widely found in synthetic drugs, natural products and Functional materials are very common, especially in pharmaceutical compounds containing heterocyclic or fused rings. Therefore, the development of such compounds plays an important role in the design and synthesis of drugs and their intermediates. The traditional synthesis method of pyridine compounds mainly involves the condensation reaction of carbonyl compounds, but this method has some limitations, such as poor substrate expansion. In recent years, in order to improve the limitations of such methods, many researchers have developed a variety of pyridine compounds preparation process. |
application | 2-(4-nitrophenyl) pyridine can be used as an intermediate in pharmaceutical synthesis. |