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N-(2-Bromopropyl)-N-ethyl-9H-fluoren-9-amine bromide

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Identification
Molecular formula
C16H19BrN
CAS number
1318021-32-6
IUPAC name
2-bromopropyl-ethyl-(9H-fluoren-9-yl)ammonium;bromide
State
State

In its typical form, it is a solid with a white to off-white appearance.

Melting point (Celsius)
152.00
Melting point (Kelvin)
425.15
Boiling point (Celsius)
324.60
Boiling point (Kelvin)
597.80
General information
Molecular weight
322.17g/mol
Molar mass
322.1650g/mol
Density
1.5200g/cm3
Appearence

This compound typically appears as a solid at room temperature. It may present as a white to off-white crystalline powder.

Comment on solubility

Solubility of 2-bromopropyl-ethyl-(9H-fluoren-9-yl)ammonium bromide (C16H19BrN)

The solubility of 2-bromopropyl-ethyl-(9H-fluoren-9-yl)ammonium bromide is an intricate topic influenced by various factors. This compound can be categorized as a quaternary ammonium salt, which typically exhibits interesting solubility characteristics. Here are some key points to consider:

  • Water Solubility: Quaternary ammonium salts often exhibit good solubility in water due to the presence of positively charged ammonium ions, which can interact favorably with polar water molecules.
  • Organic Solvents: These compounds tend to be soluble in organic solvents as well; for instance, they might dissolve in acetone or ethanol owing to their molecular structure.
  • Temperature Dependency: The solubility of 2-bromopropyl-ethyl-(9H-fluoren-9-yl)ammonium bromide may vary with temperature. Typically, increased temperature leads to increased solubility.
  • pH Influence: The solubility may also be affected by the pH of the solution, as changes in acidity can alter the ionization state of the compound.

In summary, while 2-bromopropyl-ethyl-(9H-fluoren-9-yl)ammonium bromide generally displays good solubility in both water and selected organic solvents, its solubility characteristics are nuanced and influenced by environmental factors. Understanding these behaviors is essential for applications in synthesis and formulation.

Interesting facts

Interesting Facts about 2-Bromopropyl-Ethyl-(9H-Fluoren-9-yl)ammonium Bromide

2-Bromopropyl-ethyl-(9H-fluoren-9-yl)ammonium bromide is a fascinating compound that showcases intriguing properties relevant to both organic chemistry and material science. Here are some notable points:

  • Unique Structure: The presence of the fluorenyl group provides a distinctive framework, which can influence the compound's reactivity and interaction with other molecules.
  • Applications: This compound is often studied for its potential applications in organic synthesis, especially as a reagent or catalyst in chemical reactions.
  • Research Significance: Due to its quaternary ammonium structure, it plays a critical role in various biochemical studies, including investigations on microbial resistance and cell membrane interactions.
  • Fluorene Derivative: The fluorenyl moiety, derived from the polycyclic aromatic hydrocarbon fluorene, can impart unique electronic properties, making such compounds interesting for use in optoelectronic devices.
  • Reactive Characteristics: The bromine atom in its structure makes this compound reactive in nucleophilic substitution reactions, a vital aspect when considering its potential applications in synthesis.

As a chemical scientist or student, one might argue that compounds like 2-bromopropyl-ethyl-(9H-fluoren-9-yl)ammonium bromide exemplify the interface of organic chemistry with materials science, opening doors to innovative research avenues.

In summary, this compound not only offers a compelling study in structural chemistry but also opens up discussions on its multifaceted applications in modern scientific research and technology.

Synonyms
N-(2-Bromopropyl)-N-ethyl-9-fluorenamine hydrobromide
12665-51-9
AT 8
FLUOREN-9-AMINE, N-(2-BROMOPROPYL)-N-ETHYL-, HYDROBROMIDE