6115-65-7 Usage
Chemical class
Cycloheptaquinoline derivatives
Explanation
The compound belongs to a group of chemical compounds known as cycloheptaquinoline derivatives, which are characterized by a seven-membered ring fused to a quinoline ring.
Explanation
The compound is a chlorinated derivative of the parent compound 1,4-dimethyl-7,8,9,10-tetrahydro-6H-cyclohepta[b]quinoline, meaning it has a chlorine atom added to the structure.
3. Potential pharmaceutical applications
Explanation
Due to its structural properties and biological activities, the compound may have potential uses in the pharmaceutical industry.
Explanation
The compound may exhibit various pharmacological properties, such as reducing inflammation, providing pain relief, or inhibiting the growth of microorganisms.
Explanation
The compound could be utilized in the development of new therapeutic agents, potentially leading to the creation of innovative medications.
Explanation
The compound's unique structure and potential medicinal properties make it a valuable candidate for use in chemical research and drug discovery processes.
Explanation
The molecular formula represents the compound's composition, indicating the number of carbon (C), hydrogen (H), chlorine (Cl), and nitrogen (N) atoms present in the molecule.
Explanation
The compound's structure includes a chlorine atom at the 11th position, two methyl groups at the 1st and 4th positions, and a tetrahydro-6H-cyclohepta[b]quinoline core, which is a seven-membered ring fused to a quinoline ring.
Explanation
The solubility of the compound in different solvents (e.g., water, organic solvents) may vary due to its molecular structure and functional groups.
Explanation
The compound's stability could be affected by factors such as light, heat, or moisture, which may lead to degradation or alteration of its chemical structure.
Explanation
The compound can be synthesized through different chemical reactions and synthetic routes, which may involve the formation of the cycloheptaquinoline core, introduction of the chloro and methyl substituents, and other functional group modifications.
Chlorinated derivative
1,4-dimethyl-7,8,9,10-tetrahydro-6H-cyclohepta[b]quinoline
Pharmacological properties
Anti-inflammatory, analgesic, or antimicrobial effects
Development of therapeutic agents
Novel therapeutic agents
Utilization in chemical research
Unique structure and potential medicinal properties
Structural features
11-chloro substitution, 1,4-dimethyl groups, and a tetrahydro-6H-cyclohepta[b]quinoline core
Solubility
May vary depending on the solvent
Stability
May be sensitive to light, heat, or moisture
Syntheses
Various synthetic routes may be employed
Check Digit Verification of cas no
The CAS Registry Mumber 6115-65-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,1 and 5 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6115-65:
(6*6)+(5*1)+(4*1)+(3*5)+(2*6)+(1*5)=77
77 % 10 = 7
So 6115-65-7 is a valid CAS Registry Number.
