CAS 1427392-00-4
:Methyl 3-aminoimidazo[1,2-a]pyridine-7-carboxylate
Description:
Methyl 3-aminoimidazo[1,2-a]pyridine-7-carboxylate is a heterocyclic organic compound characterized by its imidazo and pyridine ring structures, which contribute to its biological activity and potential pharmaceutical applications. The presence of an amino group and a carboxylate moiety enhances its reactivity and solubility in various solvents, making it suitable for diverse chemical reactions. This compound typically exhibits moderate to high polarity due to the functional groups, which can influence its interaction with biological targets. Its molecular structure suggests potential applications in medicinal chemistry, particularly in the development of compounds with antimicrobial or anticancer properties. Additionally, the methyl ester group may facilitate further chemical modifications, allowing for the synthesis of derivatives with tailored biological activities. As with many heterocycles, the compound's stability and reactivity can be influenced by environmental factors such as pH and temperature, which are important considerations in both laboratory and industrial settings. Overall, Methyl 3-aminoimidazo[1,2-a]pyridine-7-carboxylate represents a valuable scaffold for further research and development in the field of organic and medicinal chemistry.
Formula:C9H9N3O2
InChI:InChI=1S/C9H9N3O2/c1-14-9(13)6-2-3-12-7(10)5-11-8(12)4-6/h2-5H,10H2,1H3
InChI key:InChIKey=QAAQCCZXLNWSPS-UHFFFAOYSA-N
SMILES:NC=1N2C(C=C(C(OC)=O)C=C2)=NC1
Synonyms:- Methyl 3-aminoimidazo[1,2-a]pyridine-7-carboxylate
- Imidazo[1,2-a]pyridine-7-carboxylic acid, 3-amino-, methyl ester
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Found 1 products.
Methyl 3-aminoimidazo[1,2-a]pyridine-7-carboxylate
CAS:Versatile small molecule scaffoldFormula:C9H9N3O2Purity:Min. 95%Molecular weight:191.19 g/mol
