2-(5-hydroxybenzothiophen-3-yl)acetic acid
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- Molecular formula
- C10H8O3S
- CAS Number
- 52172-29-7
- IUPAC Name
- 2-(5-hydroxybenzothiophen-3-yl)acetic acid
- Molecular Weight
- 208.25g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.4195g/cm3
- Synonyms
- 16304-48-6
Identification
Interesting facts
Interesting Facts about 2-(5-hydroxybenzothiophen-3-yl)acetic acid
2-(5-hydroxybenzothiophen-3-yl)acetic acid is a fascinating chemical compound with unique properties and potential applications. Here are some intriguing aspects to consider:
- Benzothiophene Backbone: The compound features a benzothiophene structure, which is known for its presence in various natural products and synthetic compounds. This particular framework contributes to the compound's distinct chemical behavior.
- Hydroxyl Group Activity: The presence of a hydroxyl (–OH) group enhances the compound's reactivity, making it a potential candidate for diverse chemical reactions. Hydroxyl groups are often involved in hydrogen bonding, influencing solubility and boiling behavior.
- Biological Relevance: Compounds related to benzothiophene have shown various biological activities, including anti-inflammatory and anti-cancer properties. This raises exciting research possibilities for 2-(5-hydroxybenzothiophen-3-yl)acetic acid in medicinal chemistry.
- Versatile Applications: Given its unique structure, this compound can be explored in applications ranging from pharmaceuticals to agrochemicals. The potential for use in developing new therapeutic agents is particularly promising.
- Research Implications: Ongoing studies may uncover further insights about this compound's mechanisms and interactions, possibly leading to novel discoveries in the realm of organic chemistry.
In conclusion, 2-(5-hydroxybenzothiophen-3-yl)acetic acid stands out not only for its complex structure but also for its potential applications in various scientific fields. Its exploration could yield significant benefits in advancing both basic and applied research.