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5-bromo-N,N-diethyl-4,7-dimethyl-6,6a,8,9-tetrahydroindolo[4,3-fg]quinoline-9-carboxamide

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Identification
Molecular formula
C23H26BrN3O
CAS number
98169-58-7
IUPAC name
5-bromo-N,N-diethyl-4,7-dimethyl-6,6a,8,9-tetrahydroindolo[4,3-fg]quinoline-9-carboxamide
State
State

The compound is typically a solid at room temperature, often appearing as a crystalline filement.

Melting point (Celsius)
183.30
Melting point (Kelvin)
456.45
Boiling point (Celsius)
327.50
Boiling point (Kelvin)
600.65
General information
Molecular weight
430.49g/mol
Molar mass
430.3470g/mol
Density
1.1894g/cm3
Appearence

This compound typically appears as a crystalline solid, which may range in color from white to off-white.

Comment on solubility

Solubility of 5-bromo-N,N-diethyl-4,7-dimethyl-6,6a,8,9-tetrahydroindolo[4,3-fg]quinoline-9-carboxamide

The solubility of the compound 5-bromo-N,N-diethyl-4,7-dimethyl-6,6a,8,9-tetrahydroindolo[4,3-fg]quinoline-9-carboxamide is an intriguing aspect that can influence its practical applications and formulations. Here’s what we know about its solubility characteristics:

  • Polarity: The presence of polar functional groups, such as the carboxamide, often enhances solubility in polar solvents, while the hydrophobic indole moiety can limit solubility in water.
  • Solvent Choice: Typically, this compound may exhibit better solubility in organic solvents like dimethyl sulfoxide (DMSO) or ethanol compared to water.
  • pH Influence: Solubility can potentially be altered by pH, particularly if the carboxamide group can ionize under certain conditions, making the compound more soluble in aqueous solutions.
  • Temperature Effects: As with many organic compounds, solubility may increase with temperature, allowing for greater dissolution in heated solvents.

In conclusion, understanding the solubility of this compound is essential for its use in chemical research and applications. It can often be described as solubility-restricted in water, yet promising in various organic solvents, showcasing the nuanced nature of solubility in organic chemistry.

Interesting facts

Interesting Facts about 5-bromo-N,N-diethyl-4,7-dimethyl-6,6a,8,9-tetrahydroindolo[4,3-fg]quinoline-9-carboxamide

This compound is a fascinating member of the indole family, known for its complex structure and potential bioactivity. Here are some key points:

  • Structural Significance: The structure features a tetrahydroindole core, which contributes to its unique chemical properties. The presence of multiple methyl and ethyl substituents adds to its steric complexity.
  • Pharmacological Potential: Compounds like this one have shown promise in medicinal chemistry. Their structures often allow for interactions with various biological targets, potentially leading to therapeutic applications.
  • Bromination: The incorporation of the bromine atom may enhance the compound's reactivity and its ability to engage in diverse chemical reactions, making it a useful analog in research.
  • Indole Compounds: Indole derivatives are known for their diverse biological activities, including antimicrobial, anti-inflammatory, and even anti-cancer properties. This compound could contribute to this rich area of study.

As a chemistry student or scientist, understanding the nuances of such compounds can open up exciting avenues for research in organic synthesis and pharmacology. Exploring the interactions and functionalities of this compound paves the way for innovative drug discovery.

In the words of renowned chemist Linus Pauling, “The best way to have a good idea is to have lots of ideas.” So, let’s keep exploring the depths of chemical compounds like this one!

Synonyms
SCHEMBL25890499
NSC186064
NSC-186064