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2-Ethoxyethyl carbamate

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Identification
Molecular formula
C5H11NO3
CAS number
7433-97-6
IUPAC name
2-ethoxyethyl carbamate
State
State

At room temperature, 2-Ethoxyethyl carbamate remains in a liquid state. It maintains its liquidity in most indoor conditions and should be stored in a sealed container to prevent evaporation or degradation.

Melting point (Celsius)
-37.00
Melting point (Kelvin)
236.15
Boiling point (Celsius)
220.20
Boiling point (Kelvin)
493.35
General information
Molecular weight
131.16g/mol
Molar mass
131.1560g/mol
Density
1.0760g/cm3
Appearence

2-Ethoxyethyl carbamate is typically observed as a colorless liquid. It is clear and may have a faint characteristic odor. Its appearance does not significantly change with varying ambient conditions, as long as it is kept in a controlled environment.

Comment on solubility

Solubility of 2-ethoxyethyl carbamate

2-ethoxyethyl carbamate, with the chemical formula C5H11NO3, exhibits unique solubility characteristics that are important for its applications in various fields. Here are some key points regarding its solubility:

  • Polar Nature: Due to the presence of both ethyl ether and carbamate functional groups, 2-ethoxyethyl carbamate is generally polar.
  • Solvent Compatibility: It is soluble in water as well as in organic solvents such as ethanol and acetone, making it versatile for different uses.
  • Temperature Effects: Like many chemical compounds, the solubility may increase with temperature. Therefore, higher temperatures can facilitate better dissolution in solvents.
  • pH Influence: The solubility can also be affected by the pH of the solution, as acids or bases may alter the ionization state of the molecule.

In summary, 2-ethoxyethyl carbamate's solubility can be influenced by its polar nature and compatibility with various solvents. Understanding these characteristics is crucial for optimizing its use in chemical formulations and applications.

Interesting facts

Interesting Facts About 2-Ethoxyethyl Carbamate

2-Ethoxyethyl carbamate, often referred to as an important intermediate in organic synthesis, is a compound that holds significant value in the field of chemistry due to its versatile applications. Here are some fascinating insights about this compound:

  • Versatile Applications: 2-ethoxyethyl carbamate is commonly used in the production of plastics, resins, and other polymers, contributing to the manufacturing of materials used in various industries.
  • Polymer Chemistry: The compound is also important in polymer chemistry, where it serves as a building block for creating sophisticated materials with tailored properties.
  • Synthesis and Reactivity: As a carbamate, it can react with various nucleophiles, making it a useful intermediate for synthesizing a range of chemical structures.
  • Biological Significance: Some studies indicate potential biological activity, which spurs interest in exploring its effects as a pharmaceutical agent or in medicinal chemistry.

Overall, 2-ethoxyethyl carbamate represents the encounter of simplicity and complexity in organic chemistry, making it a subject of ongoing research and application. As a compound that merges utility and intrigue, it continues to attract attention in both academic and industrial settings.

In the words of a chemistry student, "Understanding compounds like 2-ethoxyethyl carbamate enriches our comprehension of chemical interactivity and opens doors to innovation!"

Synonyms
628-65-9
CARBAMIC ACID, (2-ETHOXYETHYL) ESTER
2-Ethoxyethanol carbamate
Ethoxyethyl-carbamate
(2-Ethoxyethyl)carbamate
Ethanol, 2-ethoxy-, carbamate
BRN 1753554
SCHEMBL4240446
DTXSID70211888
AKOS006272802