Skip to main content

Ethyl N-(3-carbamoyloxypropyl)carbamate

ADVERTISEMENT
Identification
Molecular formula
C8H16N2O4
CAS number
177039-39-3
IUPAC name
ethyl N-(3-carbamoyloxypropyl)carbamate
State
State

At room temperature, ethyl N-(3-carbamoyloxypropyl)carbamate is a solid. It is stable under normal conditions and should be stored in a cool, dry place.

Melting point (Celsius)
52.00
Melting point (Kelvin)
325.00
Boiling point (Celsius)
295.00
Boiling point (Kelvin)
568.00
General information
Molecular weight
218.24g/mol
Molar mass
218.2410g/mol
Density
1.1800g/cm3
Appearence

Ethyl N-(3-carbamoyloxypropyl)carbamate appears as a white crystalline solid. It is often supplied in powder form and is characterized by its fine granules.

Comment on solubility

Solubility of Ethyl N-(3-carbamoyloxypropyl)carbamate

Ethyl N-(3-carbamoyloxypropyl)carbamate is a unique compound with a distinct solubility profile influenced by its chemical structure. Understanding its solubility is essential for applications in various fields such as pharmaceuticals and agrochemicals.

Key Factors Influencing Solubility

  • Polarity: The presence of polar functional groups such as the carbamate and carbamoyl moieties enhances the overall polarity of the molecule, likely leading to better solubility in polar solvents.
  • Hydrogen Bonding: The ability to form hydrogen bonds with water molecules can significantly increase solubility. Ethyl N-(3-carbamoyloxypropyl)carbamate's structure suggests it may engage in such interactions.
  • Chain Length: The length of the hydrocarbon chain impacts solubility; longer chains may reduce solubility in water but can enhance solubility in organic solvents.

In general, the solubility of such compounds can be summarized as follows:

  1. Good solubility in polar solvents: Due to its polar characteristics.
  2. Moderate solubility in non-polar solvents: The presence of long-chain alkyl groups can lead to some degree of solubility.
  3. Temperature Dependency: Solubility is likely to increase with temperature, a common behavior in many organic compounds.

In conclusion, while empirical data on the solubility of ethyl N-(3-carbamoyloxypropyl)carbamate will provide a clearer picture, its structural features suggest that it is soluble in a variety of solvents, primarily polar ones. This solubility behavior can play a crucial role in its effectiveness and application in practical scenarios.

Interesting facts

Interesting Facts about Ethyl N-(3-carbamoyloxypropyl)carbamate

Ethyl N-(3-carbamoyloxypropyl)carbamate, a fascinating chemical compound, belongs to the family of carbamates, which are known for their diverse applications in agriculture, pharmaceuticals, and chemical synthesis. Here are some intriguing aspects of this compound:

  • Biochemical Significance: Compounds of the carbamate family are often used in the development of pharmaceuticals, especially in drugs targeting the nervous system due to their ability to inhibit certain enzymes.
  • Versatile Use: The presence of both ethyl and carbamoyloxy groups in its structure allows this compound to interact in a variety of chemical reactions, making it a component of interest in research and industrial applications.
  • Research Potential: Studies have shown that carbamate derivatives can exhibit unique biological activity, providing a pathway for the discovery of new therapeutic agents.
  • Environmental Considerations: Like many carbamate compounds, understanding the environmental impact of ethyl N-(3-carbamoyloxypropyl)carbamate is crucial, as its breakdown products could potentially affect ecological systems.

As a scientist or chemistry student, it's essential to appreciate the intricate balance between potential benefits and risks associated with such compounds. The study of ethyl N-(3-carbamoyloxypropyl)carbamate not only deepens our knowledge of organic chemistry but also sheds light on the innovative ways we can harness chemical compounds for the betterment of society.

Synonyms
Ethyl (3-carbamoyloxypropyl)carbamate
5659-67-6
BRN 1949539
CARBAMIC ACID, (3-HYDROXYPROPYL)-, ETHYL ESTER, CARBAMATE