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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

Name5-Bromo-2-methyl-4-pyrimidinecarboxylic acid
Synonyms2-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

Molecular FormulaC6H5BrN2O2
Molarmassa217.02
Täthet1.795±0.06 g/cm3(Predicted)
Melting Point172-173 °C (decomp)(Solv: methanol (67-56-1))
Boling Point335.2±27.0 °C(Predicted)
Blixtpunkt156.505°C
Vapor Presure0mmHg at 25°C
pKa1.53±0.10(Predicted)
LagringstillståndSealed in dry,Room Temperature
Refractive Index1.61

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

Användningar 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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