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6H-Thiochromeno[4,3-b]quinoline

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Identification
Molecular formula
C15H11NS
CAS number
81-52-9
IUPAC name
6H-thiochromeno[4,3-b]quinoline
State
State

At room temperature, 6H-Thiochromeno[4,3-b]quinoline is typically a solid.

Melting point (Celsius)
245.00
Melting point (Kelvin)
518.00
Boiling point (Celsius)
450.00
Boiling point (Kelvin)
723.00
General information
Molecular weight
239.33g/mol
Molar mass
239.3300g/mol
Density
1.3000g/cm3
Appearence

6H-Thiochromeno[4,3-b]quinoline appears as a solid, most commonly seen in forms like powders or crystals. The compound's specific color and form can depend on purity and specific conditions of synthesis.

Comment on solubility

Solubility of 6H-thiochromeno[4,3-b]quinoline

When it comes to the solubility of 6H-thiochromeno[4,3-b]quinoline, several factors play a pivotal role in determining how this intriguing compound interacts with various solvents. Understanding its solubility characteristics can shed light on its potential applications in both industrial and research settings.

Key Factors Influencing Solubility:

  • Polarity: The degree of polarity of the compound affects its solubility in polar vs. non-polar solvents. 6H-thiochromeno[4,3-b]quinoline may demonstrate varied solubility depending on the solvent used.
  • Temperature: Increasing temperature generally enhances solubility for most compounds. Therefore, examining how 6H-thiochromeno[4,3-b]quinoline dissolves at different temperatures can provide useful insights.
  • pH Levels: The pH of the solution can influence the dissolution process, especially if the compound has acidic or basic functional groups.

As with many organic compounds, 6H-thiochromeno[4,3-b]quinoline might show limited solubility in water, a characteristic shared by compounds with larger organic structures. On the other hand, it could exhibit better solubility in organic solvents such as ethanol or dimethyl sulfoxide (DMSO), which can solvate its complex structure effectively.

In conclusion, the solubility of 6H-thiochromeno[4,3-b]quinoline is a multifaceted subject tied to its chemical nature and external environmental conditions. By exploring this aspect, researchers can better anticipate the compound's behavior in various applications.

Interesting facts

Interesting Facts about 6H-thiochromeno[4,3-b]quinoline

The compound 6H-thiochromeno[4,3-b]quinoline is an intriguing member of the thiochromene and quinoline family, showcasing a fascinating blend of structural features. This compound is primarily recognized for its diverse applications and potential in various fields:

  • Versatile Applications: Due to its unique structure, this compound has been explored for applications in organic synthesis, pharmaceuticals, and materials science.
  • Biological Activity: Some studies suggest that derivatives of this compound may display biological activities, including antimicrobial and anticancer properties, which makes it a subject of interest in medicinal chemistry.
  • Fluorescence Properties: The thiochromene structure contributes to its interesting photophysical properties, which can be exploited in developing fluorescent sensors and dye materials.
  • Research Ongoing: Ongoing research into 6H-thiochromeno[4,3-b]quinoline aims to uncover more of its potential applications, especially in novel drug discovery.

In the realm of synthetic organic chemistry, compounds like 6H-thiochromeno[4,3-b]quinoline serve as valuable building blocks. Its synthesis often involves the fusion of a thiochromene moiety with a quinoline fragment, which can lead to exciting derivatives with enhanced properties.

As we explore the avenues of modern chemistry, one might say, "The possibilities are as vast as the structures we can create." The collaboration between chemistry, biology, and material science through compounds like this exemplifies the multidisciplinary nature of scientific exploration.

Synonyms
225-57-0
6H-(1)BENZOTHIOPYRANO(4,3-b)QUINOLINE
BRN 0187735
6H-[1]Benzothiopyrano[4,3-b]quinoline
DTXSID40177023
DTXCID6099514