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Carvedilol

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Identification
Molecular formula
C24H26F3N1O3
CAS number
72956-09-3
IUPAC name
N,N-dimethyl-3-[5-(trifluoromethyl)-1,2,3,4-tetrahydrocarbazol-9-yl]propan-1-amine
State
State

Carvedilol is typically in a solid state at room temperature.

Melting point (Celsius)
114.00
Melting point (Kelvin)
387.20
Boiling point (Celsius)
569.20
Boiling point (Kelvin)
842.20
General information
Molecular weight
406.49g/mol
Molar mass
406.4870g/mol
Density
1.2806g/cm3
Appearence

Carvedilol is typically a white to off-white crystalline powder.

Comment on solubility

Solubility of N,N-dimethyl-3-[5-(trifluoromethyl)-1,2,3,4-tetrahydrocarbazol-9-yl]propan-1-amine

N,N-dimethyl-3-[5-(trifluoromethyl)-1,2,3,4-tetrahydrocarbazol-9-yl]propan-1-amine, often characterized by its complex structure, exhibits intriguing solubility properties:

  • Polar Characteristics: The presence of the trifluoromethyl group and the amine component indicates a level of polarity, which may enhance its solubility in polar solvents such as water and alcohols.
  • Hydrophobic Interactions: Conversely, the bulky tetrahydrocarbazole moiety contributes to hydrophobic characteristics, likely diminishing solubility in highly polar environments.
  • Solvent Compatibility: This compound is expected to be more soluble in organic solvents like dichloromethane or ethanol, as these can better accommodate hydrophobic interactions.
  • Temperature Dependency: As with many organic compounds, solubility may increase with temperature, promoting the dissolution in various solvents.

In summary, while N,N-dimethyl-3-[5-(trifluoromethyl)-1,2,3,4-tetrahydrocarbazol-9-yl]propan-1-amine demonstrates notable solubility characteristics, its actual solubility will significantly depend on the solvent used and the environmental conditions, making it a compound of interest for studies on solubility dynamics.

Interesting facts

Interesting Facts about N,N-Dimethyl-3-[5-(Trifluoromethyl)-1,2,3,4-tetrahydrocarbazol-9-yl]propan-1-amine

N,N-dimethyl-3-[5-(trifluoromethyl)-1,2,3,4-tetrahydrocarbazol-9-yl]propan-1-amine is a fascinating compound that exemplifies the intricate world of organic chemistry. This compound boasts a unique structure and a range of applications that make it notable in both academic and practical settings.

Key Features

  • Trifluoromethyl Group: The trifluoromethyl (-CF3) group attached to the tetrahydrocarbazole moiety significantly influences the compound's chemical behavior, enhancing its lipophilicity and biological activity.
  • Tetrahydrocarbazole Structure: Derived from carbazole, this structure provides potential for interesting *electronic properties* and engages in various reactions thanks to its nitrogen-containing framework.
  • Diverse Applications: Compounds like this are often researched in fields such as pharmaceuticals, materials science, and agrochemicals, particularly due to their potential as *bioactive molecules* or *ligands* in coordination chemistry.

Applications in Research

The unique combination of functional groups in N,N-dimethyl-3-[5-(trifluoromethyl)-1,2,3,4-tetrahydrocarbazol-9-yl]propan-1-amine opens the door for exciting research opportunities:

  • Pharmacological Studies: Compounds with similar structures are often studied for their potential in treating various medical conditions.
  • Material Science: The electronic properties imparted by the trifluoromethyl and carbazole moieties make it a good candidate for use in electronic devices or sensors.

As a compound that resides at the intersection of *organic synthesis* and *practical applications*, N,N-dimethyl-3-[5-(trifluoromethyl)-1,2,3,4-tetrahydrocarbazol-9-yl]propan-1-amine is a great illustration of how chemical ingenuity can lead to the development of materials that may change the world of science as we know it.