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4,5,6,7-Tetrahydrobenzothiophene

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Identification
Molecular formula
C8H10S
CAS number
1003-10-5
IUPAC name
4,5,6,7-tetrahydrobenzothiophene
State
State
4,5,6,7-Tetrahydrobenzothiophene is a liquid at room temperature, which facilitates its use in various chemical syntheses and industrial applications.
Melting point (Celsius)
-44.00
Melting point (Kelvin)
229.15
Boiling point (Celsius)
187.00
Boiling point (Kelvin)
460.15
General information
Molecular weight
126.21g/mol
Molar mass
126.2140g/mol
Density
1.1300g/cm3
Appearence
4,5,6,7-Tetrahydrobenzothiophene typically appears as a colorless to pale yellow liquid. It has an aromatic odor characteristic of thiophene compounds.
Comment on solubility

Solubility of 4,5,6,7-Tetrahydrobenzothiophene

4,5,6,7-Tetrahydrobenzothiophene, with a chemical formula of C9H11S, is an interesting compound concerning its solubility characteristics. Understanding solubility is crucial for various applications, especially in organic synthesis and pharmaceutical development. Here are some key points about its solubility:

  • Polarity: 4,5,6,7-tetrahydrobenzothiophene is a non-polar to slightly polar molecule due to the presence of carbon and sulfur atoms.
  • Solvent Compatibility: It demonstrates solubility in organic solvents such as hexane, toluene, and ethanol, while being relatively insoluble in water.
  • Temperature Influence: The solubility generally increases with temperature in organic solvents, making it easier to dissolve at higher temperatures.
  • Practical Applications: Due to its solubility profile, it can be utilized in various organic reactions where non-polar solvents are advantageous.

In summary, while 4,5,6,7-tetrahydrobenzothiophene has limited solubility in polar solvents like water, it is soluble in a range of organic solvents, providing versatility in applications. Understanding its solubility properties is essential for effectively utilizing this compound in chemical processes.

Interesting facts

Interesting Facts about 4,5,6,7-tetrahydrobenzothiophene

4,5,6,7-tetrahydrobenzothiophene is an intriguing compound that belongs to the class of heterocyclic compounds, particularly featuring a fused ring system. Here are some captivating insights about this unique chemical:

  • Structural Diversity: The compound consists of both a benzene ring and a thiophene ring fused together, leading to a variety of geometric and electronic properties that are significant in different chemistry applications.
  • Pharmaceutical Potential: Compounds with a similar structure have shown promise in medicinal chemistry. They may serve as templates for developing new pharmaceutical agents, especially in the context of treating neurological disorders.
  • Material Science Applications: Due to its unique ring structure, 4,5,6,7-tetrahydrobenzothiophene can also be explored for its potential in organic electronics, such as semiconductor materials and conductors.
  • Reactivity: The presence of sulfur within the thiophene portion can influence the compound's reactivity, making it a point of interest for synthetic organic chemistry.
  • Research Use: It can be utilized in a variety of synthetic pathways, serving as an intermediate or starting material for producing other complex organic compounds.

In summary, 4,5,6,7-tetrahydrobenzothiophene is not just another heterocycle; it represents an intersection of multiple scientific disciplines, showcasing the interplay between structure and function in organic chemistry. As researchers continue to explore its potential, this compound may open new avenues for innovation in both medicine and materials science.

Synonyms
BRN 1237239
6435-76-3
BENZOTHIOPHENE, 4,5,6,7-TETRAHYDRO-
4,5,6,7-Tetrahydro-2-benzothiophene
DTXSID00214569
5-17-01-00498 (Beilstein Handbook Reference)
DTXCID80137060
13129-17-4
4,5,6,7-tetrahydro-1-benzothiophene
4,5,6,7-Tetrahydrobenzo[b]thiophene
Benzo[b]thiophene, 4,5,6,7-tetrahydro-
4,5,6,7-tetrahydrobenzothiophene
MFCD19442759
SCHEMBL75265
SCHEMBL18435208
CBKDCOKSXCTDAA-UHFFFAOYSA-N
ALBB-027003
AC8430
AKOS016025623
AS-8899
SY230069
DB-348896
CS-0444568