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CAS 5447-47-2

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2,3-dihydro-1H-cyclopenta[b]quinoline-9-carboxylic acid

Description:
2,3-Dihydro-1H-cyclopenta[b]quinoline-9-carboxylic acid, with the CAS number 5447-47-2, is a bicyclic compound that features a quinoline structure fused with a cyclopentane ring. This compound typically exhibits characteristics common to heterocyclic compounds, including potential biological activity due to its nitrogen-containing ring system. It is likely to be a solid at room temperature and may have moderate solubility in organic solvents, depending on the presence of functional groups. The carboxylic acid moiety suggests that it can participate in acid-base reactions and may form salts or esters. Additionally, the compound may exhibit fluorescence or other optical properties, making it of interest in various applications, including pharmaceuticals and materials science. Its structural features may also contribute to specific interactions with biological targets, which could be explored for medicinal chemistry applications. However, detailed studies would be necessary to fully understand its reactivity, stability, and potential uses.
Formula:C13H11NO2
InChI:InChI=1/C13H11NO2/c15-13(16)12-8-4-1-2-6-10(8)14-11-7-3-5-9(11)12/h1-2,4,6H,3,5,7H2,(H,15,16)
SMILES:c1ccc2c(c1)c(c1CCCc1n2)C(=O)O
Synonyms:
  • 1H-cyclopenta[b]quinoline-9-carboxylic acid, 2,3-dihydro-
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