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5-Bromo-2-methyl-4-pyrimidinecarboxylic acid

5-Bromo-2-methyl-4-pyrimidinecarboxylic acid - Names and IdentifiersName5-Bromo-2-methyl-4-pyri

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5-Bromo-2-methyl-4-pyrimidinecarboxylic acid - Names and Identifiers

Nama5-Bromo-2-methyl-4-pyrimidinecarboxylic acid
Sinonim2-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-
CAS100707-39-9
InChIInChI=1/C6H5BrN2O2/c1-3-8-2-4(7)5(9-3)6(10)11/h2H,1H3,(H,10,11)

5-Bromo-2-methyl-4-pyrimidinecarboxylic acid - Physico-chemical Properties

Rumus MolekulerC6H5BrN2O2
Massa Molar217.02
Kepadatan1.795±0.06 g/cm3(Predicted)
Titik Melting172-173 °C (decomp)(Solv: methanol (67-56-1))
Titik Boling335.2±27.0 °C(Predicted)
Titik Flash156.505°C
Tekanan Vapor0mmHg di 25°C
pKa1.53±0.10(Predicted)
Kondisi penyimpananTerkunci dalam kering,Suhu Kamar
Indeks Refraksi1.61

5-Bromo-2-methyl-4-pyrimidinecarboxylic acid - Reference Information

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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