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2,7-Dibromo-9H-fluoren-4-amine

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Identification
Molecular formula
C13H7Br2N
CAS number
162883-11-8
IUPAC name
2,7-dibromo-9H-fluoren-4-amine
State
State

At room temperature, 2,7-Dibromo-9H-fluoren-4-amine is in a solid state. It is typically handled as a powder and can be stably stored under standard conditions if kept dry and in a sealed container.

Melting point (Celsius)
180.00
Melting point (Kelvin)
453.15
Boiling point (Celsius)
502.00
Boiling point (Kelvin)
775.15
General information
Molecular weight
332.00g/mol
Molar mass
332.0360g/mol
Density
2.3400g/cm3
Appearence

2,7-Dibromo-9H-fluoren-4-amine typically appears as a light-yellow to off-white powder. It is crystalline in nature, and its color can vary slightly depending on the purity and specific conditions of synthesis.

Comment on solubility

Solubility of 2,7-dibromo-9H-fluoren-4-amine

The solubility of 2,7-dibromo-9H-fluoren-4-amine is influenced by its molecular structure, polar functional groups, and the surrounding environment. Generally, aromatic amines like this compound exhibit varying solubility profiles based on their substituents and the solvent used.

When considering the solubility of this compound, here are some essential points:

  • Polarity: The presence of bromine atoms introduces some polarity, which may enhance solubility in polar solvents.
  • Solvent Choice: It is likely to be more soluble in organic solvents such as ethanol and dichloromethane, while being less soluble in non-polar solvents.
  • Hydrogen Bonding: The amine group may engage in hydrogen bonding, which can facilitate solubility in polar solvents but may hinder it in some complex mixtures.

In general, for synthetic and industrial applications, understanding the solubility profile of 2,7-dibromo-9H-fluoren-4-amine is crucial for its practical use. As the old adage goes, "like dissolves like," which holds true when predicting its behavior in various chemical environments.

Interesting facts

Interesting Facts about 2,7-Dibromo-9H-Fluoren-4-amine

2,7-Dibromo-9H-fluoren-4-amine is a fascinating chemical compound that plays a significant role in various areas of chemistry and material science. Here are some intriguing aspects worth noting:

  • Structural Configuration: This compound features a unique structure comprising a fluorenyl backbone with bromine substituents at the 2 and 7 positions and an amine group at the 4 position. This arrangement contributes to its stability and reactivity.
  • Application in Organic Electronics: Due to its conjugated system, this compound finds application in the development of organic semiconductors. These materials are pivotal for the advancement of light-emitting diodes (LEDs) and organic photovoltaic cells (solar cells).
  • Fluorene Derivatives: As a derivative of fluorene, it exemplifies how small changes in molecular structure can significantly influence the properties of compounds. The bromine atoms, for example, enhance the electronic properties and can modify solubility.
  • Research Significance: Researchers employ 2,7-dibromo-9H-fluoren-4-amine in various studies, ranging from exploring new synthetic pathways to developing polymeric materials with tailored functionalities.

In the words of a renowned chemist, "The beauty of chemistry lies in the transformative power of small modifications." This compound is a prime example of how subtle changes can lead to a plethora of innovations and applications.

As studies continue, the potential applications of 2,7-dibromo-9H-fluoren-4-amine in diverse fields like photonics, sensing technologies, and drug discovery only expand, underscoring the ever-evolving nature of chemical research.

Synonyms
2,7-dibromo-9H-fluoren-4-amine
1785-09-7
2,7-Dibromo-4-fluorenamine
9H-Fluoren-4-amine, 2,7-dibromo-
FLUOREN-4-AMINE, 2,7-DIBROMO-
Y6N4Y2DN2X
NSC-91426
NSC 91426
BRN 2729752
NSC91426
UNII-Y6N4Y2DN2X
NCIOpen2_009742
Fluoren-4-amine,7-dibromo-
3-12-00-03297 (Beilstein Handbook Reference)
SCHEMBL24173294
DTXSID60170490
BS-21844
DS-012649