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CAS 872355-65-2

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Ethyl 5-amino-3-chloro-2-pyridinecarboxylate

Description:
Ethyl 5-amino-3-chloro-2-pyridinecarboxylate is a chemical compound characterized by its pyridine ring structure, which is a six-membered aromatic ring containing one nitrogen atom. This compound features an ethyl ester functional group, contributing to its solubility in organic solvents. The presence of an amino group (-NH2) and a chloro group (-Cl) on the pyridine ring enhances its reactivity and potential for forming various derivatives. The amino group can participate in hydrogen bonding and nucleophilic reactions, while the chloro group can serve as a leaving group in substitution reactions. Ethyl 5-amino-3-chloro-2-pyridinecarboxylate is of interest in medicinal chemistry and organic synthesis due to its potential biological activity and utility in the development of pharmaceuticals. Its molecular structure allows for various modifications, making it a versatile intermediate in chemical synthesis. As with many nitrogen-containing heterocycles, it may exhibit unique properties such as varying solubility and reactivity depending on the surrounding functional groups and the overall molecular environment.
Formula:C8H9ClN2O2
InChI:InChI=1S/C8H9ClN2O2/c1-2-13-8(12)7-6(9)3-5(10)4-11-7/h3-4H,2,10H2,1H3
InChI key:InChIKey=UMRAOWMLHPGXOL-UHFFFAOYSA-N
SMILES:C(OCC)(=O)C1=C(Cl)C=C(N)C=N1
Synonyms:
  • Ethyl 5-amino-3-chloro-2-pyridinecarboxylate
  • 2-Pyridinecarboxylic acid, 5-amino-3-chloro-, ethyl ester
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