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Fluorenylbromide

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Identification
Molecular formula
C16H18Br2N
CAS number
51932-85-9
IUPAC name
2-bromoethyl-ethyl-(9H-fluoren-9-yl)ammonium;bromide
State
State
Fluorenylbromide is a solid at room temperature, typically appearing as a stable lattice of crystalline bodies.
Melting point (Celsius)
112.00
Melting point (Kelvin)
385.00
Boiling point (Celsius)
280.00
Boiling point (Kelvin)
553.00
General information
Molecular weight
356.20g/mol
Molar mass
356.2040g/mol
Density
1.7080g/cm3
Appearence

Fluorenylbromide appears as a white crystalline solid. It is usually found in powder or crystalline form and has no color in its pure state.

Comment on solubility

Solubility of 2-Bromoethyl-ethyl-(9H-fluoren-9-yl)ammonium Bromide

The solubility of 2-bromoethyl-ethyl-(9H-fluoren-9-yl)ammonium bromide can be influenced by several factors due to its organic nature and the presence of the ammonium and bromide ions. Here are some important points to consider:

  • Polarity: The presence of the bromide ion often increases solubility in polar solvents, such as water, while the larger organic moiety may restrict solubility in nonpolar solvents.
  • Temperature: Like many chemical compounds, its solubility can increase with rising temperatures, enhancing interactions with solvent molecules.
  • pH Sensitivity: Being an ammonium salt, its solubility may also be affected by changes in pH, potentially influencing its ionization and thus its interaction with the solvent.

As a general rule, ammonium bromides tend to exhibit good solubility in aqueous solutions, making this compound likely soluble in polar solvents. However, the actual solubility might vary significantly based on the precise conditions under which it is used.

In summary, consider the following factors for solubility:

  1. Solvent Type: Polar solvents will generally be more favorable.
  2. Temperature Conditions: Higher temperatures usually improve solubility.
  3. pH Levels: The solubility may shift with different pH levels.

Understanding these conditions will be instrumental when predicting the behavior of this compound in various chemical environments.

Interesting facts

Interesting Facts About 2-Bromoethyl-ethyl-(9H-fluoren-9-yl)ammonium Bromide

2-Bromoethyl-ethyl-(9H-fluoren-9-yl)ammonium bromide is a fascinating compound in the realm of organic and medicinal chemistry. Here are some intriguing aspects of this compound:

  • Versatile Applications: This compound is often employed as a reagent in various chemical reactions, particularly in the synthesis of more complex molecules. Its unique structure allows researchers to explore diverse chemical pathways.
  • Fluorene Backbone: The presence of the fluorene moiety contributes to fascinating optical properties, making it useful in OLED (Organic Light Emitting Diodes) technologies and fluorescence studies.
  • Ammonium Group: The ammonium group in its structure plays a crucial role in its solubility and interaction with biological systems, thereby making it a compound of interest for drug development.
  • Polyfunctional Opportunities: The bromoethyl group provides sites for further substitution, opening up countless possibilities for chemists eager to modify this compound for tailored applications.
  • Scientific Interest: Researchers are drawn to exploring the compound's potential in different fields, including materials science, medicinal chemistry, and even environmental chemistry due to its functional versatility.

As one delves deeper into organic synthesis and material science, compounds like 2-bromoethyl-ethyl-(9H-fluoren-9-yl)ammonium bromide serve as crucial building blocks, driving innovation and expanding our understanding of complex chemical systems. Its study exemplifies the beauty of chemical ingenuity, illustrating how even a single compound can unlock a multitude of research avenues!

Synonyms
N-(2-Bromoethyl)-N-ethylfluoren-9-amine hydrobromide
12774-27-5
AT 2
FLUOREN-9-AMINE, N-(2-BROMOETHYL)-N-ETHYL-, HYDROBROMIDE