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

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

Courriel : info@standard-groups.com

Contenu

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

Nom	5-Bromo-2-methyl-4-pyrimidinecarboxylic acid
Synonymes	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)

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

Formule moléculaire	C6H5BrN2O2
Masse molaire	217.02
Densité	1.795±0.06 g/cm3(Predicted)
Point de fusion	172-173 °C (decomp)(Solv: methanol (67-56-1))
point Boling	335.2±27.0 °C(Predicted)
Point d'éclair	156.505°C
pression vapeur	0 mmHg à 25°C
Le PKA	1.53±0.10(Predicted)
Condition de stockage	Scellé à sec, température ambiante
Indice de réfraction	1.61

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

Utilisations

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

Disclaimer: Le contenu ci-dessus est destiné à des fins de référence et de communication uniquement entre les initiés de l'industrie, et ne garantit pas son exactitude ou son exhaustivité. Conformément aux lois et règlements pertinents et aux règlements de ce site Web, les unités ou personnes qui achètent des articles connexes doivent obtenir des qualifications et des conditions de qualification valides.

Précédent :L-histidine dihydrochloride

Page suivante:3-(Chloromethyl)-5-methylpyridine hydrochloride