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Benzothiophen-3-ol

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Identification
Molecular formula
C8H6OS
CAS number
7327-62-4
IUPAC name
benzothiophen-3-ol
State
State

At room temperature, Benzothiophen-3-ol is a solid. It is relatively stable under normal conditions but should be handled with care due to its reactivity with strong oxidizing agents.

Melting point (Celsius)
141.00
Melting point (Kelvin)
414.15
Boiling point (Celsius)
300.00
Boiling point (Kelvin)
573.15
General information
Molecular weight
150.20g/mol
Molar mass
150.2040g/mol
Density
1.3280g/cm3
Appearence

Benzothiophen-3-ol is a pale yellow or brown solid. It is typically in crystalline form and may have an odor that is characteristic of aromatic compounds.

Comment on solubility

Solubility of Benzothiophen-3-ol

Benzothiophen-3-ol, a compound characterized by its unique structure and functional groups, exhibits moderate solubility in various solvents. When discussing its solubility, several key points can be noted:

  • Water Solubility: Benzothiophen-3-ol has limited solubility in water due to its hydrophobic aromatic structure.
  • Organic Solvent Solubility: It is more soluble in organic solvents, particularly in non-polar solvents such as benzene, ethanol, and chloroform.
  • Temperature Dependence: Solubility can change with temperature; generally, increasing the temperature enhances solubility in organic solvents.

In many scenarios, it's often quoted that “the solubility of a compound is a vital aspect of its chemical behavior.” Therefore, understanding the solubility of benzothiophen-3-ol is crucial in its applications, such as in pharmaceuticals and environmental chemistry. Research into its solubility can also provide insights into its reactivity and potential interactions with other chemical species.

Interesting facts

Interesting Facts about Benzothiophen-3-ol

Benzothiophen-3-ol is a fascinating compound that belongs to the class of heterocyclic aromatic compounds. Here are some key points to consider:

  • Structure: The compound features a benzothiophene ring fused with a hydroxyl group, making it unique among its peers. This structure contributes to its interesting chemical properties.
  • Biological Importance: Benzothiophen-3-ol has been studied for its potential biological activity. Research indicates that it may possess antioxidant and anti-inflammatory properties, which could lead to therapeutic applications.
  • Source of Interest: It is often found in various natural products, especially in plants, where it serves as a secondary metabolite. Its occurrence in nature highlights its ecological importance.
  • Industrial Applications: This compound is of interest in the chemical industry for its potential uses in developing dyes and pigments. The unique properties of benzothiophen-3-ol can lead to innovations in materials science.
  • Research Frontiers: Ongoing studies are exploring the compound's role in organic synthesis and its potential as a lead compound in drug discovery. It also serves as a model for understanding interactions in complex biological systems.

In conclusion, benzothiophen-3-ol is much more than just a chemical entity; it's a bridge linking chemistry, biology, and industry. Researchers and students alike find this compound a rich subject for exploration, offering numerous avenues for study and application.

Synonyms
3-Hydroxybenzothiophene
520-72-9
BENZO(b)THIOPHENE-3-OL
BRN 0114954
Benzo[b]thiophene-3-ol
DTXSID70199970
5-17-04-00188 (Beilstein Handbook Reference)
DTXCID30122461
xhqbiycrfvvhfd-uhfffaoysa-n
benzo[b]thiophen-3-ol
1-Benzothiophen-3-ol
Benzothiophen-3-ol
3-Hydroxythianaphthene
Thioindoxyl
MFCD01663546
1-Benzothiophen-3-ol #
SCHEMBL276823
CHEMBL3311419
AKOS003611445
DB-011514
CS-0453212