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BZP

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Identification
Molecular formula
C12H17NS
CAS number
13649-85-7
IUPAC name
2-(benzothiophen-3-yl)-N,N-dimethyl-ethanamine
State
State

The compound is generally found in a solid state at room temperature.

Melting point (Celsius)
129.00
Melting point (Kelvin)
402.20
Boiling point (Celsius)
256.60
Boiling point (Kelvin)
529.80
General information
Molecular weight
219.34g/mol
Molar mass
219.3360g/mol
Density
1.0702g/cm3
Appearence

BZP, or 1-benzylpiperazine, typically appears as a white crystalline powder. It might have differences in texture but is predominantly known in this solid form at room temperature. It is occasionally found pressed into tablets.

Comment on solubility

Solubility of 2-(benzothiophen-3-yl)-N,N-dimethyl-ethanamine (C12H17NS)

The solubility of 2-(benzothiophen-3-yl)-N,N-dimethyl-ethanamine, often abbreviated as DMET, can be intriguing due to its unique structure. This compound exhibits properties influenced by both hydrophobic (due to the benzothiophen ring) and hydrophilic (from the amine) characteristics. The solubility often depends on the following factors:

  • Polarity: Due to the presence of the amine group, DMET can engage in hydrogen bonding, potentially increasing solubility in polar solvents.
  • Hydrophobic Interactions: The large benzothiophen structure contributes to a significant hydrophobic character, which may limit solubility in water.
  • Solvent Type: Solubility is expected to be greater in organic solvents such as ethanol or DMSO, where the non-polar aromatic moiety can interact favorably.

In summary, while the compound can dissolve in polar solvents to some extent, its overall low solubility in water makes it more compatible with organic solvent systems. As a rule of thumb, hydrophobic compounds tend to fare poorly in polar solvents, so exploring various organic solvents is key for achieving optimal solubility with DMET.

Interesting facts

Interesting Facts About 2-(Benzothiophen-3-yl)-N,N-dimethyl-ethanamine

This intriguing compound, 2-(benzothiophen-3-yl)-N,N-dimethyl-ethanamine, is notable for its unique structural features and potential applications in various fields. Below are some captivating aspects of this chemical:

  • Structural Diversity: The presence of a benzothiophene moiety offers enhanced aromatic properties, making this compound stand out in the chemical landscape.
  • Psychoactive Potential: Compounds similar to this structure have been studied for their psychoactive properties. Investigating its interaction with the central nervous system can lead to breakthroughs in understanding neuropharmacology.
  • Role in Research: Studying 2-(benzothiophen-3-yl)-N,N-dimethyl-ethanamine expands our knowledge of amine compounds, particularly in medicinal chemistry where modifications to amine structures can impact biological activity.
  • Versatile Applications: This compound may show promise in developing new therapies for mental health disorders, showcasing the importance of small modifications in chemical structures for significant therapeutic benefits.
  • Synthetic Challenges: The synthesis of such compounds often requires intricate and innovative methodologies, making it an exciting area of research for synthetic chemists.

In conclusion, 2-(benzothiophen-3-yl)-N,N-dimethyl-ethanamine is not just another compound; it embodies the rich interplay between structure and function in organic chemistry. As research in this area continues, we may uncover even more fascinating properties and applications for compounds of this nature.

Synonyms
BRN 1425393
BENZO(b)THIOPHENE-3-ETHYLAMINE, N,N-DIMETHYL-
10275-64-6
N,N-Dimethylbenzo(b)thiophene-3-ethylamine
3-(2-(Dimethylamino)ethyl)benzo(b)thiophene
DTXSID80145488
DTXCID0067979
SCHEMBL25028208