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Thiochromeno[4,3-b]indole

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Identification
Molecular formula
C17H11NS
CAS number
110345-01-4
IUPAC name
thiochromeno[4,3-b]indole
State
State

At room temperature, thiochromeno[4,3-b]indole is typically in a solid state. The compound's stability and solid-state make it useful for various experimental and application-focused scenarios in the chemical and pharmaceutical industries.

Melting point (Celsius)
76.00
Melting point (Kelvin)
349.15
Boiling point (Celsius)
335.00
Boiling point (Kelvin)
608.15
General information
Molecular weight
265.35g/mol
Molar mass
265.3460g/mol
Density
1.4200g/cm3
Appearence

Thiochromeno[4,3-b]indole usually presents as a crystalline solid that can appear in various colors depending on purity and specific conditions of synthesis. Often used in chemical research and pharmaceutical studies, this compound may display different hues based on its polymorphic forms and solvates. Its exact visual appearance can vary between white, pale yellow, to brownish shades depending on conditions like humidity, temperature, and exposure to light.

Comment on solubility

Solubility of Thiochromeno[4,3-b]indole

Thiochromeno[4,3-b]indole, a fascinating heterocyclic compound, demonstrates interesting solubility characteristics that can vary significantly based on its environment. Here are some key points regarding its solubility:

  • Solvent Influence: The compound's solubility is influenced by the choice of solvent. It tends to be more soluble in polar organic solvents such as dimethyl sulfoxide (DMSO) and acetone.
  • Temperature Dependence: Like many organic compounds, increasing the temperature can enhance solubility. Heating the solvent can often dissolve larger amounts of thiochromeno[4,3-b]indole.
  • pH Effect: The solubility may also be affected by the acidity or basicity of the environment, as changes in pH can alter the compound's ionization status.

In summary, while the solubility of thiochromeno[4,3-b]indole is relatively limited in non-polar solvents, it exhibits a notable degree of solubility in polar solvents under appropriate conditions. As a rule of thumb, strong polar solvents are best for enhancing the solubility of this intriguing compound.

Interesting facts

Interesting Facts about Thiochromeno[4,3-b]indole

Thiochromeno[4,3-b]indole is a fascinating compound that has captured the attention of researchers due to its unique structure and potential applications in various fields. Here are some compelling aspects to consider:

  • Structural Complexity: This compound features an intricate fused ring system that combines elements of both thiochromene and indole. Such structural diversity not only enhances its chemical properties but also provides a rich platform for further derivatization and study.
  • Potential Biological Activities: Compounds containing indole structures, including thiochromeno[4,3-b]indole, are often explored for their biological activities. Many indole derivatives have been reported to exhibit *antimicrobial*, *antioxidant*, and *anticancer* properties, making them valuable in medicinal chemistry.
  • Reaction Versatility: The presence of sulfur in thiochromeno[4,3-b]indole may facilitate various chemical reactions, such as *Sulfenylation* or *Thioketone formation*, allowing chemists to create a range of derivatives with enhanced applications.
  • Applications in Organic Electronics: The electronic properties of thiochromeno[4,3-b]indole derivatives are being investigated for potential use in organic light-emitting diodes (OLEDs) and organic photovoltaics, showcasing its versatility beyond traditional medicinal applications.
  • Research and Development: As a subject of ongoing research, thiochromeno[4,3-b]indole is gradually revealing its potential across various scientific domains. The study of its synthetic pathways and reactivity could lead to new insights into organic reaction mechanisms.

In summary, thiochromeno[4,3-b]indole exemplifies the intersection of structural elegance and functional potential in organic chemistry. Understanding its properties and applications will not only contribute to advancements in medicinal chemistry but also potentially enhance the development of innovative electronic materials. As the quote goes, “*Chemistry is the art of problem-solving,*” and compounds like thiochromeno[4,3-b]indole certainly pose intriguing challenges and opportunities for scientists.

Synonyms
thiochromeno[4,3-b]indole
239-12-3
(1)BENZOTHIOPYRANO(4,3-b)INDOLE
Benz(b)indolo(2,3-d)thiopyran
BRN 1075508
[1]benzothiopyrano[4,3-b]indole
DTXSID40178595
SCHEMBL4492071
DTXCID00101086