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Thioflavone derivative

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Identification
Molecular formula
C22H12Cl2O2S2
CAS number
24135-86-0
IUPAC name
5-chloro-2-(5-chloro-7-methyl-3-oxo-benzothiophen-2-ylidene)-7-methyl-benzothiophen-3-one
State
State
The compound is a solid at room temperature

It remains stable in its solid crystalline form and is typically stored in a cool, dry, and well-ventilated area.

Melting point (Celsius)
258.00
Melting point (Kelvin)
531.00
Boiling point (Celsius)
400.00
Boiling point (Kelvin)
673.00
General information
Molecular weight
431.31g/mol
Molar mass
431.3060g/mol
Density
1.4980g/cm3
Appearence

This compound typically occurs as a yellow to orange crystalline powder. It exhibits a characteristic bright yellow color which is common among thioflavone derivatives, owing to its conjugated system.

Comment on solubility

Solubility of 5-chloro-2-(5-chloro-7-methyl-3-oxo-benzothiophen-2-ylidene)-7-methyl-benzothiophen-3-one

The solubility of the compound 5-chloro-2-(5-chloro-7-methyl-3-oxo-benzothiophen-2-ylidene)-7-methyl-benzothiophen-3-one, a complex benzothiophene derivative, can present notable challenges due to its intricate structure. Understanding the solubility characteristics of such compounds is crucial in various applications, particularly in medicinal chemistry and material sciences.

Key points about its solubility include:

  • Solvent Dependency: The solubility is highly influenced by the choice of solvent. Polar solvents like methanol or ethanol may improve solubility compared to nonpolar solvents like hexane.
  • Temperature Effects: As with many organic compounds, increasing the temperature tends to enhance solubility, promoting better dissolution in solvents.
  • Functional Groups Impact: The presence of halogen atoms and keto groups in the structure may facilitate interactions with solvents, although steric hindrance may also inhibit solubility.

In conclusion, while the specific solubility value for C16H12Cl2O2S may not be readily available in literature, it can be anticipated that the solubility behavior is complex, requiring systematic investigation under varied conditions. Understanding these factors provides valuable insight for its practical applications and formulations.

Interesting facts

Interesting Facts about 5-chloro-2-(5-chloro-7-methyl-3-oxo-benzothiophen-2-ylidene)-7-methyl-benzothiophen-3-one

This intriguing compound belongs to the class of benzothiophenes, which are known for their diverse biological activities. The complex structure of 5-chloro-2-(5-chloro-7-methyl-3-oxo-benzothiophen-2-ylidene)-7-methyl-benzothiophen-3-one offers various points of interest:

  • Diverse Applications: Benzothiophene derivatives, including this compound, often find applications in pharmaceuticals and agrochemicals. Their ability to act as intermediates and building blocks makes them valuable in synthetic organic chemistry.
  • Biological Significance: Many benzothiophene derivatives exhibit promising anti-cancer, anti-inflammatory, and antimicrobial properties, paving the way for potential therapeutic agents.
  • Structural Complexity: This compound features multiple functional groups, contributing to its potential reactivity and biological interaction mechanisms. The presence of chlorine atoms and ketone functionality enhances its molecular versatility.
  • Synthesis Challenges: The synthesis of such complex organic compounds can often pose significant challenges, requiring advanced synthetic methods and strategies to achieve the desired purity and yield.
  • Research Focus: Ongoing research concentrates on elucidating the mechanisms of action of benzothiophenes, which may unlock new pathways for medicinal chemistry development.

In summary, 5-chloro-2-(5-chloro-7-methyl-3-oxo-benzothiophen-2-ylidene)-7-methyl-benzothiophen-3-one is much more than a mere chemical formula. It represents a potential treasure trove for scientific inquiry, bridging the gap between synthetic chemistry and practical applications in health and agriculture.

Synonyms
5-chloro-2-(5-chloro-7-methyl-3-oxo-1-benzothiophen-2-ylidene)-7-methyl-1-benzothiophen-3-one
5-chloro-2-(5-chloro-7-methyl-3-oxobenzo[b]thien-2(3H)-ylidene)-7-methylbenzo[b]thiophene-3(2H)-one
ANTHRA RED B
Benzo[b]thiophen-3(2H)-one, 5-chloro-2-(5-chloro-7-methyl-3-oxobenzo[b]thien-2(3H)-ylidene)-7-methyl-
DTXSID8063919
HUGACAUYNJDGTB-UHFFFAOYSA-N
NS00013529