Name | 6,8-dibromoimidazo[1,2-a]pyrazine |
Synonyms | 8-dibroMoiMidazo[1 6,8-Dibromimidazo[1,2-a]pyrazin 6,8-dibromoimidazo[1,2-a]pyrazine 6,8-DIBROMOIMIDAZO[1,2-A]PYRAZINE 6,8-Dibromoimidazol[1,2-a]pyrazine IMidazo[1,2-a]pyrazine, 6,8-dibroMo- Imidazo[1,2-a]pyrazine, 6,8-dibromo- |
CAS | 63744-22-9 |
EINECS | 811-059-4 |
InChI | InChI=1/C6H3Br2N3/c7-4-3-11-2-1-9-6(11)5(8)10-4/h1-3H |
Molecular Formula | C6H3Br2N3 |
Molar Mass | 276.92 |
Density | 2.35±0.1 g/cm3(Predicted) |
Melting Point | 165.0 to 169.0 °C |
Water Solubility | Slightly soluble in water. |
pKa | -0.36±0.30(Predicted) |
Storage Condition | under inert gas (nitrogen or Argon) at 2-8°C |
Refractive Index | 1.802 |
MDL | MFCD08460056 |
Use | This product is for scientific research only and shall not be used for other purposes. |
Application | 6, 8-dibromoimidazolo [1,2a] pyrazine is an important pharmaceutical intermediate, 6, 8-dibromo-imidazolo [1,2-A] pyrazine can also be used to prepare novel compounds for organic electroluminescent devices with improved performance. |
preparation | 2-amino -3,5-dibromopyrazine (2.53g,10mmol), chloroacetaldehyde (1.96g, 10mmol) and acetonitrile 10ml were added to a 50mL single-mouth round bottom flask. The mixture in the reaction flask was stirred for 10 hours at 80°C. TLC and GC determined that the reaction was complete. after the reaction, the solvent was removed by spin evaporation to obtain the crude product, and the pure product 6, 8-dibromoimidazolium and [1,2a] pyrazine was separated by silica gel column chromatography. after drying, the yield was calculated to be 61.73%, the purity was 98.30%(HPLC), and the melting point was 114 ℃-117 ℃. Nuclear magnetic resonance analysis: 1HNMR(400Hz, deuterated chloroform) δ:8.288(d,1H),7.887(dd,1H),7.793(dd,1H). |