Dimethylaminoethyl diphenylcarbamate

Identification

Molecular formula

C₁₈H₂₂N₂O₂

CAS number

538-91-2

IUPAC name

2-(dimethylamino)ethyl N,N-diphenylcarbamate

State

At room temperature, Dimethylaminoethyl diphenylcarbamate is typically in a solid state, appearing as crystalline granules or powder. Its state facilitates easy handling and measurement for experimental and synthetic applications.

Melting point (Celsius)

53.50

Melting point (Kelvin)

326.65

Boiling point (Celsius)

398.00

Boiling point (Kelvin)

671.15

General information

Molecular weight

312.39g/mol

Molar mass

312.3880g/mol

Density

1.1010g/cm³

Appearence

Dimethylaminoethyl diphenylcarbamate typically appears as a crystalline solid. It can vary from an off-white powder to a slightly yellow solid depending on its purity and specific crystalline form. Handling should be done carefully to prevent moisture uptake, as this can alter its physical characteristics.

Comment on solubility

Solubility of 2-(dimethylamino)ethyl N,N-diphenylcarbamate

The solubility of 2-(dimethylamino)ethyl N,N-diphenylcarbamate in various solvents is a fascinating aspect of its chemical behavior. Its unique structure significantly influences its solubility characteristics:

Polar solvents: The presence of the dimethylamino group can enhance solubility in polar solvents like water. However, the bulky diphenyl group may hinder complete hydration.
Non-polar solvents: In contrast, 2-(dimethylamino)ethyl N,N-diphenylcarbamate is expected to exhibit good solubility in non-polar organic solvents due to its hydrophobic segments.
Competing interactions: Factors such as temperature and the nature of impurities can significantly alter solubility. For instance, elevated temperatures often increase solubility due to enhanced molecular movement.

It is important to consider that "like dissolves like," which is a fundamental rule in solubility. Therefore, understanding both the polar and non-polar characteristics of 2-(dimethylamino)ethyl N,N-diphenylcarbamate is essential for predicting its behavior in different environments.

In summary, while this compound exhibits interesting solubility properties varying between polar and non-polar environments, proper experimentation is necessary to determine its specific solubility limits in various conditions.

Interesting facts

Interesting Facts about 2-(Dimethylamino)ethyl N,N-Diphenylcarbamate

2-(Dimethylamino)ethyl N,N-diphenylcarbamate is an intriguing compound that finds a significant role in the field of organic chemistry and medicinal applications. Here are some noteworthy aspects of this compound:

Biological Activity: This compound exhibits potential biological activity, making it a subject of interest in pharmacology. Its derivatives are explored for their effectiveness in various medicinal applications.
Structure Diversity: The presence of a dimethylamino group and two phenyl rings contributes to the structural diversity of this compound. The electronic properties of these groups can influence its reactivity and interactions.
Use as a Carbamate: As a carbamate derivative, it’s utilized in the synthesis of pesticides, herbicides, and various pharmaceuticals, showcasing its industrial relevance.
Research Applications: Scientists have been investigating this compound for its potential as a catalyst in organic reactions, emphasizing its utility in synthetic chemistry.
Safety Considerations: While exploring its properties, researchers pay close attention to the safety profiles of such compounds, as some carbamates can exhibit toxicity and environmental concerns.

As a specialized subject of study, 2-(dimethylamino)ethyl N,N-diphenylcarbamate serves as a reminder of the intricate connections between molecular structure and function. It highlights the continuous exploration within the realms of chemistry and potential therapeutic landscapes.