2-(Benzothiophen-3-yl)ethanamine

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Identification

Molecular formula
C10H11NS
CAS Number
53984-36-0
IUPAC Name
2-(benzothiophen-3-yl)ethanamine
Molecular Weight
179.27g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.2000g/cm3
Synonyms
14585-66-1
Interesting facts

Interesting Facts about 2-(benzothiophen-3-yl)ethanamine

2-(benzothiophen-3-yl)ethanamine, a fascinating organic compound, showcases a unique combination of both thienyl and aromatic structures which significantly influences its properties and applications. Below are some intriguing highlights:

  • Structural Diversity: This compound belongs to the family of ethylamines and is characterized by the presence of a benzothiophene moiety, contributing to its intriguing chemical behavior.
  • Biological Activity: Compounds like 2-(benzothiophen-3-yl)ethanamine have been studied for their potential pharmacological applications. Research indicates they may play a role in modulating neurotransmitter systems, making them of interest in medicinal chemistry.
  • Synthetic Routes: The synthesis of this compound can involve several synthetic methods, including the use of transition metal-catalyzed reactions and nucleophilic substitutions, showcasing the versatility of modern organic synthesis techniques.
  • Potential Applications: Beyond medicinal uses, compounds with similar structures have been explored for their role in organic electronics, particularly in the development of conductive polymers and organic semiconductors.

As a chemistry student or researcher, exploring 2-(benzothiophen-3-yl)ethanamine can provide valuable insights into the complexities of organic synthesis and the intricate relationship between molecular structure and biological function. This compound exemplifies the *beauty of chemistry*, where every molecule has the potential to unlock new discoveries in science and technology.

As the renowned chemist Linus Pauling once said, "The best way to have a good idea is to have lots of ideas." This sentiment rings true as we delve deeper into compounds like 2-(benzothiophen-3-yl)ethanamine, sparking curiosity and innovative thinking in the world of chemical sciences.

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