5778-65-4

Usage

Molecular structure

The compound has a cyclohepta[b]quinoline ring system, which is a seven-membered ring fused to a quinoline ring (a tricyclic system).

Chlorine substitution

A chlorine atom is present at position 11 of the cyclohepta[b]quinoline ring system.

Methoxy substitution

A methoxy group (-OCH3) is attached at position 4 of the cyclohepta[b]quinoline ring system.

Hydrogenation

The compound is tetrahydro, meaning it has four hydrogen atoms added to the ring system, specifically at positions 7, 8, 9, and 10.

Heteroatom content

The molecule contains nitrogen in the quinoline ring and oxygen in the methoxy group.

Aromaticity

The cyclohepta[b]quinoline ring system is aromatic, which contributes to its stability and potential pharmacological properties.

Quinoline derivatives

The compound belongs to the class of quinoline derivatives, which are known for their diverse biological activities.

Potential applications

Due to its structure and belonging to the quinoline class, 11-chloro-4-methoxy-7,8,9,10-tetrahydro-6H-cyclohepta[b]quinoline may have potential uses in medicinal chemistry and drug development.

Further research

The specific uses and effects of 11-chloro-4-methoxy-7,8,9,10-tetrahydro-6H-cyclohepta[b]quinoline would depend on additional research and testing to determine its pharmacological properties and potential therapeutic applications.

Molecular weight

The molecular weight of the compound can be calculated based on its chemical formula, which would be the sum of the atomic weights of all the atoms present in the molecule.

Solubility

The solubility of the compound in various solvents (e.g., water, organic solvents) would depend on its polarity and hydrogen bonding capabilities, which in turn could influence its pharmacokinetic properties.

Stability

The stability of the compound under different conditions (e.g., temperature, pH, light exposure) would be important for its potential use in drug development and formulation.