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CAS 158980-21-3

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Ethyl 6-aminoimidazo[1,2-a]pyridine-2-carboxylate

Description:
Ethyl 6-aminoimidazo[1,2-a]pyridine-2-carboxylate is a chemical compound characterized by its unique bicyclic structure, which incorporates both an imidazole and a pyridine ring. This compound features an ethyl ester functional group, contributing to its solubility and reactivity. The presence of an amino group at the 6-position of the imidazo ring enhances its potential for hydrogen bonding and reactivity in various chemical reactions, making it a valuable intermediate in organic synthesis. The carboxylate moiety allows for further derivatization, which can be exploited in medicinal chemistry for the development of bioactive compounds. Ethyl 6-aminoimidazo[1,2-a]pyridine-2-carboxylate is of interest in pharmaceutical research due to its potential biological activities, including antimicrobial and anticancer properties. Its molecular structure and functional groups suggest that it may interact with biological targets, making it a candidate for further investigation in drug development. As with many organic compounds, proper handling and safety measures should be observed due to potential toxicity and reactivity.
Formula:C10H11N3O2
InChI:InChI=1/C10H11N3O2/c1-2-15-10(14)8-6-13-5-7(11)3-4-9(13)12-8/h3-6H,2,11H2,1H3
SMILES:CCOC(=O)c1cn2cc(ccc2n1)N
Synonyms:
  • Ethyl 6-Amino-Imidazo[1,2-A]Pyridine-2-Carboxylate
  • 6-Aminoimidazo[1,2-A]Pyridine-2-Carboxylic Acid Ethyl Ester
  • Imidazo[1,2-a]pyridine-2-carboxylic acid, 6-amino-, ethyl ester (9CI)
  • 6-Aminoimidazo[1,2-A]Pyridine-2-Carboxylic Acid Ethyl Ester, 95+%
  • 6-amino-2-imidazo[1,2-a]pyridinecarboxylic acid ethyl ester
  • Ethyl 6-aMinoiMidazo[1,2-a]pyridin-2-carboxylate
  • Ethyl 6-aminoimidazo[1,2-a]pyridine-2-carboxylate USP/EP/BP
  • 6-AMINOIMIDAZO[1,2-A]PYR
  • Imidazo[1,2-a]pyridine-2-carboxylic acid, 6-amino-, ethyl ester
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