N-(2-bromoethyl)-N-ethyl-9H-fluoren-9-amine

Identification

Molecular formula

C₁₇H₁₆BrN

CAS number

343638-97-1

IUPAC name

N-(2-bromoethyl)-N-ethyl-9H-fluoren-9-amine

State

At room temperature, N-(2-bromoethyl)-N-ethyl-9H-fluoren-9-amine is in the solid state. The compound is typically stored in a cool, dry place and handled under proper safety precautions to maintain stability.

Melting point (Celsius)

112.00

Melting point (Kelvin)

385.20

Boiling point (Celsius)

350.50

Boiling point (Kelvin)

623.70

General information

Molecular weight

335.25g/mol

Molar mass

335.2510g/mol

Density

1.3400g/cm³

Appearence

N-(2-bromoethyl)-N-ethyl-9H-fluoren-9-amine typically appears as a solid powder under standard conditions. The exact color and texture can vary based on purity and specific storage conditions.

Comment on solubility

Solubility of N-(2-bromoethyl)-N-ethyl-9H-fluoren-9-amine

The solubility of N-(2-bromoethyl)-N-ethyl-9H-fluoren-9-amine (C₁₇H₁₆BrN) is influenced by its chemical structure and the presence of certain functional groups. To understand its solubility, consider the following factors:

Polarity: The compound contains a bromine atom as well as an amine functional group, which can contribute to polar characteristics, potentially enhancing solubility in polar solvents.
Hydrophobic Nature: The fluorenyl group introduces a significant hydrophobic character, which may hinder solubility in polar solvents and increase solubility in organic solvents.
Solvent Interactions: Its solubility may be greater in non-polar solvents such as chloroform or benzene due to the presence of aromatic structures, contrasting with its behavior in aqueous solutions.

Therefore, while it may exhibit moderate solubility in certain organic solvents, it is likely to be insoluble or only sparingly soluble in water. This highlights the importance of considering both polar and non-polar interactions when predicting the solubility of organic compounds like N-(2-bromoethyl)-N-ethyl-9H-fluoren-9-amine.

In summary, the solubility of this compound can be best understood by examining its structural features:

Polarity of functional groups
Hydrophobic contributions
Interactions with various solvents

Interesting facts

Interesting Facts about N-(2-bromoethyl)-N-ethyl-9H-fluoren-9-amine

N-(2-bromoethyl)-N-ethyl-9H-fluoren-9-amine is a fascinating compound that lies at the intersection of organic chemistry and materials science. Below are several key points that highlight its intriguing characteristics:

Structural Complexity: This compound features a fluorenyl moiety, which is characterized by its polycyclic aromatic structure. This contributes to its electronic properties and potential applications in semiconductors and optoelectronics.
Reactivity: The presence of the bromoethyl group is significant as it introduces a site for nucleophilic substitution reactions. This allows for potential modifications and the synthesis of derivatives that could serve various functional roles.
Versatile Applications: Compounds like N-(2-bromoethyl)-N-ethyl-9H-fluoren-9-amine are often investigated for their role in organic synthesis, particularly in creating complex organic molecules. They may also have implications in drug development or as intermediates in the synthesis of other important chemicals.
Fluorescent Properties: Due to the presence of the fluorenyl moiety, this compound may exhibit interesting fluorescent characteristics, making it useful in applications such as sensors or imaging in biological systems.

As a chemistry student or scientist, exploring the potential of compounds like N-(2-bromoethyl)-N-ethyl-9H-fluoren-9-amine not only enhances understanding of molecular interactions but also paves the way for innovative applications in various fields. It's a prime example of how organic compounds can be engineered for specific purposes, showcasing the beauty and complexity of chemistry!