Name | 3-Chloro-2-Nitro Pyridine |
Synonyms | Chloro-2-nitropyridine 3-Chloro-2-nitropyridine 3-CHLORO-2-NITROPYRIDINE 2-NITRO-3-CHLORO PYRIDINE 3-Chloro-2-Nitro Pyridine Pyridine, 3-chloro-2-nitro- |
CAS | 54231-32-2 |
EINECS | 678-886-9 |
InChI | InChI=1/C5H3ClN2O2/c6-4-2-1-3-7-5(4)8(9)10/h1-3H |
Molecular Formula | C5H3ClN2O2 |
Molar Mass | 158.54 |
Density | 1.489±0.06 g/cm3(Predicted) |
Melting Point | 90-91°C |
Boling Point | 279.1±20.0 °C(Predicted) |
Flash Point | 122.6°C |
Solubility | soluble in Methanol |
Vapor Presure | 0.00696mmHg at 25°C |
Appearance | powder to crystal |
Color | Light yellow to Yellow to Green |
BRN | 1637069 |
pKa | -4.87±0.22(Predicted) |
Storage Condition | Room Temprature |
Refractive Index | 1.587 |
MDL | MFCD00490110 |
Risk Codes | R36/37/38 - Irritating to eyes, respiratory system and skin. R41 - Risk of serious damage to eyes R25 - Toxic if swallowed |
Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection. S36 - Wear suitable protective clothing. S45 - In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.) S39 - Wear eye / face protection. |
UN IDs | 2811 |
Packing Group | III |
Uses | 3-chloro-2-nitropyridine is a pharmaceutical intermediate that can be used to prepare a pharmaceutical composition for the treatment of osteoarthritis and a diazacarbazole derivative used in the field of organic electroluminescence. |
Preparation | There are reports in the literature that 3-chloro-2-nitropyridine can be prepared from 3-amino-2-nitropyridine through continuous flow reaction. 3-chloro-2-nitropyridine can be used to prepare a diazacarbazole derivative. Carbazole compounds have sufficiently high triplet state, good hole transport ability, photochemical stability, high carrier mobility, strong absorption in the ultraviolet light range and a band gap of about 3.20eV, and valuable blue light And other characteristics, replace and modify on the 3,6,9-position or other carbon atoms to obtain a variety of high-efficiency luminescent materials. The luminescent material obtained by bonding the carbazole-like group diazacarbazole with different groups with electron-deficient properties can also realize the triplet state and adjustable molecular orbital energy level of the material. So as to fundamentally realize the efficient recombination of carriers in organic electroluminescent devices and obtain efficient and energy-saving OLED devices. It can also be widely used in the field of organic electroluminescence. |