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CAS 21617-16-3

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5-Chloro-2,3-dihydro-4(1H)-quinolinone

Description:
5-Chloro-2,3-dihydro-4(1H)-quinolinone is a heterocyclic organic compound characterized by its quinolinone structure, which features a fused bicyclic system comprising a benzene ring and a pyridine-like ring. The presence of a chlorine atom at the 5-position contributes to its unique reactivity and potential biological activity. This compound typically appears as a solid and is soluble in organic solvents, reflecting its non-polar characteristics. It is often studied for its pharmacological properties, as quinolinones are known to exhibit a range of biological activities, including antimicrobial and anti-inflammatory effects. The compound's molecular structure allows for various functional group modifications, making it a versatile intermediate in organic synthesis. Additionally, its stability under standard laboratory conditions makes it suitable for further chemical transformations. Safety data should be consulted for handling, as with any chemical substance, to ensure proper precautions are taken due to potential toxicity or reactivity.
Formula:C9H8ClNO
InChI:InChI=1S/C9H8ClNO/c10-6-2-1-3-7-9(6)8(12)4-5-11-7/h1-3,11H,4-5H2
InChI key:InChIKey=IPGWKHAWNXWEPG-UHFFFAOYSA-N
SMILES:O=C1C=2C(=CC=CC2Cl)NCC1
Synonyms:
  • 4(1H)-Quinolone, 5-chloro-2,3-dihydro-
  • 5-Chloro-2,3-dihydro-4(1H)-quinolinone
  • 4(1H)-Quinolinone, 5-chloro-2,3-dihydro-
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