5-Bromo-2-(methylamino)ethylbenzo[b]thiophene

Identification

Molecular formula

C₁₁H₁₂BrNS

CAS number

3869-19-6

IUPAC name

2-(5-bromobenzothiophen-3-yl)-N-methyl-ethanamine

State

At room temperature, 5-Bromo-2-(methylamino)ethylbenzo[b]thiophene is in a solid state. It is typically stable under normal conditions and should be stored in a cool, dry place.

Melting point (Celsius)

60.00

Melting point (Kelvin)

333.15

Boiling point (Celsius)

351.00

Boiling point (Kelvin)

624.15

General information

Molecular weight

256.18g/mol

Molar mass

256.1810g/mol

Density

1.4000g/cm³

Appearence

5-Bromo-2-(methylamino)ethylbenzo[b]thiophene typically appears as a crystalline solid. The color can vary depending on purity and form but generally it ranges from white to light brown. The compound may have a subtle odor characteristic of organic thio compounds.

Comment on solubility

Solubility of 2-(5-bromobenzothiophen-3-yl)-N-methyl-ethanamine

The solubility of 2-(5-bromobenzothiophen-3-yl)-N-methyl-ethanamine can be influenced by several factors, primarily its structural features and molecular interactions.

Factors Affecting Solubility

Polarity: The presence of nitrogen in the molecule can impart polar characteristics, enhancing solubility in polar solvents.
Solvent Interactions: The solubility level may vary significantly between organic solvents (like ethanol, acetone) and aqueous solutions. Polar solvents may dissolve the compound more effectively due to potential hydrogen bonding.
Functional Groups: The bromobenzothiophene structure contributes to the molecule's overall hydrophobicity, which can limit solubility in water but enhance solubility in non-polar organic solvents.

In summary, while 2-(5-bromobenzothiophen-3-yl)-N-methyl-ethanamine may exhibit variable solubility profiles depending on the solvent used, it is likely to be more soluble in non-polar solvents due to its hydrophobic regions. It’s essential to consider these properties when planning experiments or applications involving this compound. Always remember, "solubility parallels the nature of the solvent!"

Interesting facts

Interesting Facts about 2-(5-bromobenzothiophen-3-yl)-N-methyl-ethanamine

This fascinating compound holds a prominent place in the world of organic chemistry, particularly due to its diverse applications in research and potential therapeutic uses. Here are some intriguing aspects to consider:

Structural Diversity: The compound features a unique structure that combines a benzothiophene moiety with an amine, allowing for interesting interactions and properties.
Pharmacological Potential: Due to the presence of the benzothiophene ring, it has garnered attention for its potential biological activities, including neuropharmacological effects.
Research Applications: This compound is valuable in the field of medicinal chemistry, serving as a building block for synthesizing more complex pharmaceutical agents.
Photochemical Properties: Its distinct structure may exhibit interesting photochemical properties, making it a candidate for studies in photodynamic therapy or light-sensitive applications.
Complex Synthesis: The synthesis of this compound can involve multiple steps, providing an exciting challenge for chemists working in organic synthesis and reaction mechanisms.

As a quote from renowned chemist Linus Pauling aptly puts it: "The best way to have a good idea is to have a lot of ideas." Exploring compounds like 2-(5-bromobenzothiophen-3-yl)-N-methyl-ethanamine enriches our understanding of chemistry and fuels innovation in drug development and material science.

This compound exemplifies how organic chemistry continually evolves, presenting opportunities for scientists to discover new properties and applications. As research progresses, we may unlock even more secrets hidden within its molecular structure!

Synonyms

Oprea1_837031

SCHEMBL10667334

AKOS019618369

AA-516/31407049

N-[2-(5-bromo-1-benzothien-3-yl)ethyl]-N-methylamine