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11-Chloro-1,4-dimethyl-7,8,9,10-tetrahydro-6H-cyclohepta[b]quinoline

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Identification
Molecular formula
C16H16ClN
CAS number
142826-10-8
IUPAC name
11-chloro-1,4-dimethyl-7,8,9,10-tetrahydro-6H-cyclohepta[b]quinoline
State
State

At room temperature, this compound exists in a solid crystalline state.

Melting point (Celsius)
168.00
Melting point (Kelvin)
441.15
Boiling point (Celsius)
355.00
Boiling point (Kelvin)
628.15
General information
Molecular weight
259.77g/mol
Molar mass
259.7780g/mol
Density
1.2400g/cm3
Appearence

The compound typically appears as a colorless to pale yellow crystalline solid. The presence of the chlorine atom in the compound can result in a distinct chlorine-like odor.

Comment on solubility

Solubility of 11-chloro-1,4-dimethyl-7,8,9,10-tetrahydro-6H-cyclohepta[b]quinoline

The solubility of 11-chloro-1,4-dimethyl-7,8,9,10-tetrahydro-6H-cyclohepta[b]quinoline in various solvents is a critical property that can influence its applications in pharmaceuticals and organic chemistry. This compound features a complex polycyclic structure, which plays a significant role in determining its solubility profile.

Typically, compounds with such intricate ring systems exhibit:

  • Low to moderate solubility in water: The presence of chlorine and the polycyclic structure may hinder extensive interaction with water molecules.
  • Better solubility in organic solvents: Solvents like ethanol, acetone, and chloroform may effectively dissolve this compound due to similar non-polar characteristics.
  • Potential variation in solubility with temperature: As is common with many organic compounds, an increase in temperature may enhance solubility.

In general, the complex nature of such compounds often leads to a solubility pattern that can be unpredictable. It is advisable to perform solubility tests using varied solvents and conditions to gain a comprehensive understanding. As a mantra in chemistry states, "Like dissolves like," meaning that the solubility is generally more favorable between substances with similar polarities.

Overall, while the solubility of 11-chloro-1,4-dimethyl-7,8,9,10-tetrahydro-6H-cyclohepta[b]quinoline may present challenges, it is crucial for its successful utilization in various chemical contexts.

Interesting facts

Interesting Facts about 11-Chloro-1,4-dimethyl-7,8,9,10-tetrahydro-6H-cyclohepta[b]quinoline

11-Chloro-1,4-dimethyl-7,8,9,10-tetrahydro-6H-cyclohepta[b]quinoline is a fascinating compound that belongs to the quinoline family, which is notable for its broad application in various fields of chemistry and pharmacology. Here are some intriguing aspects of this compound:

  • Cyclohepta[b]quinoline Framework: The compound features a unique polycyclic structure, which is a characteristic trait of quinolines, lending it potential biological activity. The fused ring system supports various interactions with biological targets.
  • Chlorine Substitution: The presence of a chlorine atom at the 11-position of the quinoline structure can influence the compound's reactivity and bioactivity, often making it a point of interest in drug design and molecular biology studies.
  • Methyl Groups: The dimethyl groups at the 1 and 4 positions may enhance the lipophilicity of the compound, which is crucial for its absorption in biological systems. As students often state, "Methylation can change the game!"
  • Potential Applications: Compounds like this have garnered attention in medicinal chemistry for their potential in developing new therapeutic agents. They may exhibit anti-inflammatory, antiviral, or anticancer properties.
  • Research Significance: Scientists studying derivatives of quinoline are excited about their aromatic stability and potential for synthesizing new compounds with altered functionalities, contributing to advancements in materials science and medicinal chemistry.

In conclusion, 11-chloro-1,4-dimethyl-7,8,9,10-tetrahydro-6H-cyclohepta[b]quinoline serves as an important reminder of how minor modifications within a compound's structure can lead to significant changes in its properties and applications. This compound not only adds a layer to the rich tapestry of quinoline derivatives but also inspires continued research into its potential benefits in various scientific domains.

Synonyms
6115-65-7
MAS 741
BRN 1576519
6H-CYCLOHEPTA(b)QUINOLINE, 7,8,9,10-TETRAHYDRO-11-CHLORO-1,4-DIMETHYL-
DTXSID60210042
7,8,9,10-Tetrahydro-11-chloro-1,4-dimethyl-6H-cyclohepta(b)quinoline
DTXCID60132533
11-chloro-1,4-dimethyl-7,8,9,10-tetrahydro-6H-cyclohepta[b]quinoline
AKOS012715920