Skip to main content

11-chloro-4-methoxy-7,8,9,10-tetrahydro-6H-cyclohepta[b]quinoline

ADVERTISEMENT
Identification
Molecular formula
C17H16ClNO
CAS number
76064-86-3
IUPAC name
11-chloro-4-methoxy-7,8,9,10-tetrahydro-6H-cyclohepta[b]quinoline
State
State

The compound is a solid at room temperature. Typically, it is encountered in a stable crystalline form due to its aromatic structure, making it relatively non-volatile compared to classic volatile organic compounds.

Melting point (Celsius)
45.00
Melting point (Kelvin)
318.15
Boiling point (Celsius)
578.50
Boiling point (Kelvin)
851.70
General information
Molecular weight
275.77g/mol
Molar mass
275.7690g/mol
Density
1.2974g/cm3
Appearence

The compound is typically observed as a yellow solid. It is a derivative of quinoline and features a cycloheptane ring fused to the quinoline structure, with a methoxy group and a chlorine atom substituent, which contribute to its specific crystalline forms.

Comment on solubility

Solubility of 11-chloro-4-methoxy-7,8,9,10-tetrahydro-6H-cyclohepta[b]quinoline

The solubility of 11-chloro-4-methoxy-7,8,9,10-tetrahydro-6H-cyclohepta[b]quinoline is an interesting aspect to consider, especially given its complex structure. The solubility is influenced by several factors:

  • Polarity: Compounds with a higher molecular weight and multiple rings tend to exhibit lower solubility in polar solvents.
  • Functional Groups: The presence of the methoxy group may provide some degree of solubility in polar solvents, while the chloro group introduces hydrophobic characteristics.
  • Hydrogen Bonding: The ability of the molecule to engage in hydrogen bonding can affect solubility as well.

In general, one can expect that:

  1. 11-chloro-4-methoxy-7,8,9,10-tetrahydro-6H-cyclohepta[b]quinoline may show limited solubility in water due to its complex cyclic structure and chlorinated derivatives.
  2. It might dissolve more readily in non-polar organic solvents such as chloroform or dichloromethane.

In summary, while the exact solubility values can vary based on experimental conditions, it is important to note that the unique structural features and the presence of functional groups in this compound play a critical role in determining its solubility profile in different solvents.

Interesting facts

Interesting Facts about 11-Chloro-4-methoxy-7,8,9,10-tetrahydro-6H-cyclohepta𝑏-quinoline

11-Chloro-4-methoxy-7,8,9,10-tetrahydro-6H-cyclohepta𝑏-quinoline is a fascinating compound that resides at the intersection of organic chemistry and medicinal research. Here are some engaging insights:

  • Structural Diversity: The compound features a unique bicyclic structure, which contributes to its biological activity. The presence of a chloro group and a methoxy group enhances its chemical reactivity and specificity.
  • Pharmacological Potential: Compounds similar to this class are of great interest in medicinal chemistry due to their potential as therapeutic agents. They may serve as leads for the development of drugs targeting various diseases.
  • Remarkable Synthesis: The synthesis of this compound involves intricate chemical reactions, showcasing the ingenuity required in organic synthesis. Techniques such as cyclization and halogenation are often employed during the production process.
  • Mechanism Exploration: Understanding how this compound interacts at the molecular level is crucial for elucidating its biological mechanisms. Research in this area can reveal critical insights into its efficacy and safety profile.

As a chemist or a student, diving into the properties and implications of 11-chloro-4-methoxy-7,8,9,10-tetrahydro-6H-cyclohepta𝑏-quinoline reveals the intricate balance of structure and function that defines much of modern chemistry. The ongoing exploration of such compounds can lead to breakthroughs in drug design and innovation.

In the words of renowned chemist Linus Pauling, "The best way to have a good idea is to have lots of ideas." In this spirit, the study of complex compounds like this one is key to advancing our understanding of chemical biology.

Synonyms
MAS 723
5778-65-4
BRN 1466941
6H-CYCLOHEPTA(b)QUINOLINE, 7,8,9,10-TETRAHYDRO-11-CHLORO-4-METHOXY-
DTXSID80206467
7,8,9,10-Tetrahydro-11-chloro-4-methoxy-6H-cyclohepta(b)quinoline
DTXCID80128958
11-chloro-4-methoxy-7,8,9,10-tetrahydro-6H-cyclohepta[b]quinoline
AKOS012716034