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CAS 17174-03-7

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2-[(4,6-DIMETHYLPYRIMIDIN-2-YL)AMINO]BENZOIC ACID

Description:
2-[(4,6-Dimethylpyrimidin-2-yl)amino]benzoic acid, with the CAS number 17174-03-7, is a chemical compound characterized by its structure, which includes a benzoic acid moiety and a pyrimidine ring. This compound features an amino group that connects the pyrimidine to the benzoic acid, contributing to its potential biological activity. The presence of two methyl groups on the pyrimidine ring enhances its lipophilicity, which may influence its solubility and interaction with biological systems. Typically, compounds of this nature may exhibit properties such as being a weak acid due to the carboxylic acid functional group, and they may participate in hydrogen bonding due to the amino and carboxylic acid functionalities. This compound may be of interest in pharmaceutical research, particularly in the development of drugs targeting specific biological pathways. Its unique structural features could also suggest potential applications in agrochemicals or as intermediates in organic synthesis. However, specific applications and biological activities would require further investigation and empirical studies.
Formula:C13H13N3O2
InChI:InChI=1/C13H13N3O2/c1-8-7-9(2)15-13(14-8)16-11-6-4-3-5-10(11)12(17)18/h3-7H,1-2H3,(H,17,18)(H,14,15,16)
SMILES:Cc1cc(C)nc(n1)Nc1ccccc1C(=O)O
Synonyms:
  • Timtec-Bb Sbb007411
  • N-(4,6-Dimethylpyrimidin-2-Yl)-2-Aminobenzoic Acid
  • Salor-Int L118710-1Ea
  • Olutasidenib Impurity 6
  • 2-[(4,6-DIMETHYLPYRIMIDIN-2-YL)AMINO]BENZOIC ACID
  • 2-[(4,6-dimethyl-2-pyrimidinyl)amino]benzoic acid
  • Benzoic acid, 2-[(4,6-dimethyl-2-pyrimidinyl)amino]-
  • N-(4,6-Dimethylpyrimidin-2-yl)anthranilic acid, 2-[(2-Carboxyphenyl)amino]-4,6-dimethylpyrimidine
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