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CAS 81633-29-6

:

5-Pyrimidinecarboxylic acid, 2-amino-4-methyl-, ethyl ester

Description:
5-Pyrimidinecarboxylic acid, 2-amino-4-methyl-, ethyl ester, also known by its CAS number 81633-29-6, is an organic compound characterized by its pyrimidine ring structure, which is a six-membered aromatic heterocycle containing two nitrogen atoms. This compound features a carboxylic acid functional group and an ethyl ester moiety, contributing to its solubility and reactivity. The presence of an amino group at the 2-position and a methyl group at the 4-position of the pyrimidine ring influences its biological activity and potential applications in pharmaceuticals and agrochemicals. Typically, such compounds exhibit moderate to high polarity due to the functional groups, which can affect their interaction with biological systems. They may also participate in hydrogen bonding, enhancing their solubility in polar solvents. The compound's structural characteristics suggest potential uses in medicinal chemistry, particularly in the development of drugs targeting various biological pathways. As with many pyrimidine derivatives, it may also exhibit antimicrobial or anti-inflammatory properties, making it of interest in research and development.
Formula:C8H11N3O2
InChI:InChI=1S/C8H11N3O2/c1-3-13-7(12)6-4-10-8(9)11-5(6)2/h4H,3H2,1-2H3,(H2,9,10,11)
InChI key:InChIKey=YBFVMJRSZCVJJP-UHFFFAOYSA-N
SMILES:C(OCC)(=O)C=1C(C)=NC(N)=NC1
Synonyms:
  • 5-Pyrimidinecarboxylic acid, 2-amino-4-methyl-, ethyl ester
  • 2-Amino-4-methylpyrimidine-5-carboxylic acid ethyl ester
  • Ethyl 2-amino-4-methylpyrimidine-5-carboxylate
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