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Dicyclohexylcarbodiimide

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Identification
Molecular formula
C13H21N3O
CAS number
538-75-0
IUPAC name
2-(diethylamino)ethyl N,N-dicyclohexylcarbamate
State
State

It is typically found as a solid under normal room temperature conditions.

Melting point (Celsius)
34.00
Melting point (Kelvin)
307.15
Boiling point (Celsius)
128.00
Boiling point (Kelvin)
401.15
General information
Molecular weight
206.33g/mol
Molar mass
206.3340g/mol
Density
0.9534g/cm3
Appearence

Dicyclohexylcarbodiimide is a white crystalline solid. It generally appears as a fine powder and is known to be moisture-sensitive. The compound is also known to have a distinct odor.

Comment on solubility

Solubility of 2-(diethylamino)ethyl N,N-dicyclohexylcarbamate

The solubility of 2-(diethylamino)ethyl N,N-dicyclohexylcarbamate is an intriguing topic, as it can influence its uses and applications in various fields. This compound, often used for its pharmacological properties, demonstrates unique solubility characteristics:

  • Polar Nature: Due to the presence of amino groups, the compound exhibits polar characteristics, which generally enhances solubility in polar solvents.
  • Hydrophobic Interactions: The dicyclohexyl portion introduces hydrophobic features, suggesting it may have limited solubility in water, a common solvent.
  • Choice of Solvents: It is expected to show better solubility in organic solvents such as ethanol, dimethyl sulfoxide (DMSO), or acetone, rather than in aqueous solutions.

In summary, the solubility of 2-(diethylamino)ethyl N,N-dicyclohexylcarbamate can be described as a balance between its polar and non-polar characteristics. As a result, while it may dissolve well in polar organic solvents, it is likely to be insoluble or sparingly soluble in water. Understanding these solubility properties is crucial for optimizing its application in scientific research and industry.

Interesting facts

Interesting Facts about 2-(Diethylamino)ethyl N,N-Dicyclohexylcarbamate

2-(Diethylamino)ethyl N,N-dicyclohexylcarbamate is a fascinating compound that belongs to the category of carbamates, which are derived from carbamic acid. This compound has garnered attention in the field of chemistry for several reasons:

  • Functional Group Diversity: Retroactively linked to both amines and esters, its structure indicates potential for diverse reactivity. The presence of diethylamino and dicyclohexyl groups allows for a wide range of chemical interactions.
  • Biological Relevance: Compounds within this class often exhibit interesting biological activities, including potential applications as pharmaceuticals or agrochemicals. Research into similar compounds has revealed their roles in enzyme inhibition!
  • Solubility and Reactivity: The unique nature of its functional groups can influence solubility in various solvents, which is crucial for reaction conditions and product yields in synthetic chemistry.
  • Versatile Applications: Given the relative abundance of carbamates in various industries—from herbicides to pharmaceuticals—this compound may find use in areas such as medicinal chemistry or materials science.
  • Structural Insights: The dicyclohexyl component offers steric hindrance, which can greatly affect the kinetics and mechanism of reactions involving this compound. Understanding these factors is key for chemists looking to design new experiments.

As chemists continue to explore the reactivity and applications of 2-(diethylamino)ethyl N,N-dicyclohexylcarbamate, they uncover greater insights not just into its practical uses, but also into fundamental principles of organic chemistry. The study of such compounds illustrates the intricate relationships between structure and function, revealing the complex layer of interactions at play in chemical systems.