5-Bromo-2-methyl-4-pyrimidinecarboxylic acid - Names and IdentifiersName5-Bromo-2-methyl-4-pyri
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Nome | 5-Bromo-2-methyl-4-pyrimidinecarboxylic acid |
Sinonimi | 2-Methyl-5-bromopyrimidine-4-carboxylicaci 5-Bromo-2-methylpyrimidin-4-carboxylic acid 5-Bromo-2-methylpyrimidine-4-carboxylic acid 5-Bromo-2-methyl-4-pyrimidinecarboxylic acid 2-methyl-5-bromopyrimidine-4-carboxylic acid 4-Pyrimidinecarboxylic acid, 5-bromo-2-methyl- 4-PyriMidinecarboxylic acid, 5-broMo-2-Methyl- |
CAS | 100707-39-9 |
InChI | InChI=1/C6H5BrN2O2/c1-3-8-2-4(7)5(9-3)6(10)11/h2H,1H3,(H,10,11) |
Formula molecolare | C6H5BrN2O2 |
massa molare | 217.02 |
Densità | 1.795±0.06 g/cm3(Predicted) |
Punto di fusione | 172-173 °C (decomp)(Solv: methanol (67-56-1)) |
punto Boling | 335.2±27.0 °C(Predicted) |
Punto Flash | 156.505°C |
Pressione del vapore | 0mmHg at 25°C |
pKa | 1.53±0.10(Predicted) |
Condizioni di conservazione | Sigillato in secco, temperatura ambiente |
Indice di rifrattività | 1.61 |
Usi | 2-methyl-5-bromopyrimidin-4-carboxylic acid is a useful research chemical for organic synthesis and other chemical processes. Pyrimidine compounds are widely found in the human body and organisms. The development of such compounds has been paid attention to by the pharmaceutical and pesticide circles. |
Preparation | Using 2,4-dimethyl-5-bromopyrimidine as the starting material, under alkaline conditions, potassium permanganate is oxidized to prepare the target compound 2-methyl-5-bromopyrimidin-4-carboxylic acid [1]. Or using 3, 4-dibromo-5-hydroxyfuran-2 (5h)-one as the starting material, and forming a pyrimidine ring with acetamidine hydrochloride to prepare 2-methyl-5-bromopyrimidine-4-carboxylic acid. The synthesis reaction formula of 2-methyl-5-bromopyrimidin-4-carboxylic acid is as follows: Figure 1 Synthesis reaction formula of 2-methyl-5-bromopyrimidin-4-carboxylic acid |
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