Name | 2-Bromo-5-iodopyridine |
Synonyms | 2-BROMO-5-IODOPYRIDINE 2-Bromo-5-iodopyridine 2-Bromo-5-Iodine Pyridine Pyridine, 2-bromo-5-iodo- |
CAS | 73290-22-9 |
EINECS | 629-182-5 |
InChI | InChI=1/C5H3BrIN/c6-5-2-1-4(7)3-8-5/h1-3H |
InChIKey | LLKRSJVPTKFSLS-UHFFFAOYSA-N |
Molecular Formula | C5H3BrIN |
Molar Mass | 283.89 |
Density | 2.347±0.06 g/cm3(Predicted) |
Melting Point | 121-123 °C (lit.) |
Boling Point | 278.6±20.0 °C(Predicted) |
Flash Point | 122.3°C |
Vapor Presure | 0.00714mmHg at 25°C |
Appearance | White solid |
Color | White to off-white |
BRN | 109100 |
pKa | -1.23±0.10(Predicted) |
Storage Condition | Keep in dark place,Sealed in dry,Room Temperature |
Sensitive | Light Sensitive |
Refractive Index | 1.665 |
MDL | MFCD03095201 |
Risk Codes | R22 - Harmful if swallowed R37/38 - Irritating to respiratory system and skin. R41 - Risk of serious damage to eyes |
Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36/39 - |
WGK Germany | 3 |
HS Code | 29333990 |
Hazard Class | IRRITANT |
introduction | 2-bromo -5-iodopyridine is white or off-white solid powder under normal temperature and pressure, which can be soluble in common organic solvents, such as dimethyl sulfoxide, N,N-dimethyl formamide, dichloromethane, ethyl acetate, methanol, ethanol and other alcohol solvents, but the solubility in water is poor. It can be used as an intermediate in organic synthesis. |
use | 2-bromo-5-iodopyridine is a common organic synthesis intermediate, mainly used for pyridine-containing drug molecules and bioactive molecules Structural modification and derivatization. Among them, the iodine and bromine on the pyridine ring can be obtained by Suzuki coupling reaction, and the pyridine ring is connected to the product of the aromatic ring at positions 2 and 5. |
Synthesis method | For the synthesis of 2-bromo-5-iodopyridine, the conventional synthesis method is Starting from 2, 5-dibromopyridine, use n-butyl lithium to remove the bromine on the pyridine ring to obtain the corresponding aryl lithium reagent, then add iodine to obtain the target product 2-bromo-5-iodopyridine. |