Name | 5-Bromo-2-methylpyrimidine |
Synonyms | 5-Bromo-2-methylpyrimidine 5-Bromo-2-methyl-Pyrimidine 5-BROMO-2-METHYL-PYRIMIDINE 5-bromo-2-methyl-pyrimidi... 5-Bromo-2-methyl-1,3-diazine PyriMidine, 5-broMo-2-Methyl- 2-methyl-5-bromo-1,3-pyrimidine |
CAS | 7752-78-5 |
EINECS | 691-361-9 |
InChI | InChI=1/C5H5BrN2/c1-4-7-2-5(6)3-8-4/h2-3H,1H3 |
Molecular Formula | C5H5BrN2 |
Molar Mass | 173.01 |
Density | 1.596±0.06 g/cm3(Predicted) |
Melting Point | 80.0 to 85.0 °C |
Boling Point | 195.2±13.0 °C(Predicted) |
Flash Point | 71.885°C |
Solubility | soluble in Methanol |
Vapor Presure | 0.593mmHg at 25°C |
Appearance | Solid |
Color | Light yellow to Brown |
Maximum wavelength(λmax) | ['266nm(EtOH)(lit.)'] |
pKa | 0.46±0.22(Predicted) |
Storage Condition | Inert atmosphere,2-8°C |
Refractive Index | 1.558 |
Hazard Symbols | Xi - Irritant |
Application | 2-methyl-5-bromopyrimidine is a common organic Synthon, it can be used as a molecular backbone to participate in the synthetic modification of bioactive molecules. |
prepare | a dry 10-liter 4-neck round-bottom flask was blown with nitrogen and allowed to maintain an inert atmosphere of nitrogen, A solution of 5-bromo-2-iodopyrimidine (590g, 2.07 mol) was dissolved in tetrahydrofuran (3 L). 1 M dimethylzinc solution (3.1 1 L,3.11 mol) was slowly added dropwise with stirring at 0 °c, and then Pd (PPh3) was added to the reaction system. 4(120g, 104 mmol). The resulting solution was stirred at 0°C for 3 hours, quenched by addition of 600 aqueous NH4Cl, and the resulting solution was extracted with 2 x 1.5 L EtOAc. The organic extracts were combined, dried over anhydrous magnesium sulfate and concentrated by spin-drying under vacuum. The product is obtained by purification of the residue by chromatography on SiO2 (1:50 EtOAc/petroleum ether). |