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N-(3-bromophenyl)-1H-imidazo[4,5-g]quinazolin-8-amine

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Identification
Molecular formula
C16H11BrN6
CAS number
257878-97-4
IUPAC name
N-(3-bromophenyl)-1H-imidazo[4,5-g]quinazolin-8-amine
State
State

At room temperature, this compound is in a solid state. It is typically quite stable and may be handled under standard conditions.

Melting point (Celsius)
243.50
Melting point (Kelvin)
516.65
Boiling point (Celsius)
670.15
Boiling point (Kelvin)
943.15
General information
Molecular weight
344.20g/mol
Molar mass
344.1690g/mol
Density
1.7900g/cm3
Appearence

The compound is typically a solid at room temperature and may appear as a crystalline powder.

Comment on solubility

Solubility of N-(3-bromophenyl)-1H-imidazo[4,5-g]quinazolin-8-amine

N-(3-bromophenyl)-1H-imidazo[4,5-g]quinazolin-8-amine (C16H11BrN6), a complex organic compound, exhibits intriguing solubility characteristics. Understanding the solubility of this compound is essential in various chemical applications. Here’s what you need to know:

  • Solvent Dependence: The solubility of this compound can vary significantly based on the solvent used. For instance, it may have greater solubility in organic solvents such as dimethyl sulfoxide (DMSO) or acetone compared to water.
  • Temperature Influence: Like many compounds, solubility is often affected by temperature. Increased temperatures typically facilitate improved solubility for many organic compounds.
  • Polarity Considerations: The presence of the bromine atom and nitrogen-containing rings contributes to its polarity, affecting interactions with solvents. This could lead to higher solubility in polar solvents but limited solubility in non-polar environments.

In summary, the solubility of N-(3-bromophenyl)-1H-imidazo[4,5-g]quinazolin-8-amine is influenced by factors such as:

  1. Type of solvent
  2. Temperature
  3. Polarity of the compound

As a rule of thumb, when experimenting with this compound, always consider these factors for optimal solubility outcomes. “The right solvent can turn a challenging compound into a soluble partner in reactions.”

Interesting facts

Interesting Facts About N-(3-bromophenyl)-1H-imidazo[4,5-g]quinazolin-8-amine

N-(3-bromophenyl)-1H-imidazo[4,5-g]quinazolin-8-amine is a fascinating compound that stands out due to its unique structure and potential applications in various fields. Here are some intriguing aspects:

  • Pharmaceutical Potential: Compounds with imidazoquinazolines have garnered attention within the pharmaceutical industry, particularly for their roles as potential therapeutics against cancer and infectious diseases.
  • Tailored Properties: The presence of the bromine atom enhances the compound's reactivity and may help in modifying its pharmacokinetic properties, making it an interesting candidate for drug development.
  • Structure Complexity: This compound features a complex heterocyclic structure that combines both imidazole and quinazoline rings, offering insights into the rich chemistry of nitrogen-containing heterocycles.
  • Research Interest: Studies focusing on this type of compound often explore mechanisms of action at the molecular level, which can lead to the discovery of new drugs targeting specific biological pathways.
  • Comparative Studies: Researchers frequently compare the effectiveness of imidazoquinazolines with other compounds to evaluate their medicinal benefits, enhancing our understanding of structure-activity relationships.

In conclusion, N-(3-bromophenyl)-1H-imidazo[4,5-g]quinazolin-8-amine serves as an excellent representative of the intricate and diverse world of synthetic organic compounds. Its unique features make it a subject of ongoing research and a promising candidate for future pharmaceutical advancements.

Synonyms
N-(3-bromophenyl)-1H-imidazo[4,5-g]quinazolin-8-amine
CHEMBL66031
171179-32-1
bpiq-ii
Imidazoquinazoline deriv. 8
Anilinopyrimidine deriv. 7a
BDBM3570
SCHEMBL13898313
DTXSID20274367
HSCI1_000062
BRD-K35473459-001-01-7
8-[(3-Bromophenyl)amino]-1H-imidazo[4,5-g]quinazoline