5-Bromo-2-methyl-4-pyrimidinecarboxylic acid - Names and IdentifiersName5-Bromo-2-methyl-4-pyri
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Nama | 5-Bromo-2-methyl-4-pyrimidinecarboxylic acid |
Sinonim | 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) |
Rumus Molekuler | C6H5BrN2O2 |
Massa Molar | 217.02 |
Kepadatan | 1.795±0.06 g/cm3(Predicted) |
Titik Melting | 172-173 °C (decomp)(Solv: methanol (67-56-1)) |
Titik Boling | 335.2±27.0 °C(Predicted) |
Titik Flash | 156.505°C |
Tekanan Vapor | 0mmHg di 25°C |
pKa | 1.53±0.10(Predicted) |
Kondisi penyimpanan | Terkunci dalam kering,Suhu Kamar |
Indeks Refraksi | 1.61 |
Penggunaan | 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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