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CAS 5396-25-8

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6,9-Dichloro-1,2,3,4-tetrahydroacridine

Description:
6,9-Dichloro-1,2,3,4-tetrahydroacridine is an organic compound characterized by its bicyclic structure, which includes a fused acridine ring system. This compound features two chlorine substituents at the 6 and 9 positions of the acridine framework, contributing to its unique chemical properties. It is a colorless to pale yellow solid at room temperature and is known for its potential applications in medicinal chemistry, particularly in the development of drugs targeting neurological disorders. The presence of the tetrahydro group indicates that it is a saturated derivative of acridine, which can influence its reactivity and interaction with biological systems. Additionally, the dichloro substitution can enhance its lipophilicity, affecting its pharmacokinetic properties. The compound is typically handled with care due to the presence of chlorine atoms, which can impart toxicity and environmental concerns. As with many organic compounds, its solubility, stability, and reactivity can vary based on the solvent and conditions used in experiments or applications.
Formula:C13H11Cl2N
InChI:InChI=1/C13H11Cl2N/c14-8-5-6-10-12(7-8)16-11-4-2-1-3-9(11)13(10)15/h5-7H,1-4H2
InChI key:InChIKey=UPHWUTWIUIWUJB-UHFFFAOYSA-N
SMILES:ClC=1C=2C(N=C3C1CCCC3)=CC(Cl)=CC2
Synonyms:
  • Acridine, 6,9-dichloro-1,2,3,4-tetrahydro-
  • NSC 1227
  • 6,9-Dichloro-1,2,3,4-tetrahydroacridine
  • See more synonyms
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