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(1-ethynylcyclohexyl) N-carbamoylcarbamate

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Identification
Molecular formula
C10H13N2O3
CAS number
>1202044-20-9
IUPAC name
(1-ethynylcyclohexyl) N-carbamoylcarbamate
State
State

At room temperature, this compound exists in a solid state. Its crystalline nature ensures that it maintains its form unless exposure conditions are applied that may induce phase changes, such as increased temperature beyond its melting point.

Melting point (Celsius)
152.00
Melting point (Kelvin)
425.15
Boiling point (Celsius)
376.00
Boiling point (Kelvin)
649.15
General information
Molecular weight
197.22g/mol
Molar mass
197.2230g/mol
Density
1.2100g/cm3
Appearence

The compound (1-ethynylcyclohexyl) N-carbamoylcarbamate typically appears as a white crystalline solid. Its crystalline nature allows it to form structured, solid masses that can often reflect light, lending it a somewhat shiny appearance. Under ambient conditions, its solid form is stable, maintaining its structure and not readily interacting with the surrounding atmosphere unless exposed to reactive substances.

Comment on solubility

Solubility of (1-ethynylcyclohexyl) N-carbamoylcarbamate

The solubility of (1-ethynylcyclohexyl) N-carbamoylcarbamate can be influenced by a variety of factors. Since it features both aromatic and aliphatic components, its solubility characteristics may differ significantly depending on the solvent medium.

Key points to consider include:

  • Solvent Polarity: Generally, organic compounds with similar structure tend to dissolve well in non-polar solvents due to the principle of "like dissolves like." This means (1-ethynylcyclohexyl) N-carbamoylcarbamate may show higher solubility in hydrocarbons.
  • Hydrogen Bonding: The presence of the carbamate group suggests potential for hydrogen bonding with solvents, particularly in polar solvents like water or alcohols. This can enhance solubility under specific conditions.
  • Cyclic Structure Effects: The cyclohexyl group may influence steric factors that can also impact solubility, limiting interactions with certain solvents.

Overall, for practical applications, it is essential to perform experimental solubility tests to determine the most appropriate solvents for (1-ethynylcyclohexyl) N-carbamoylcarbamate. As with many organic compounds, variations in temperature, pH, and concentration can modify solubility significantly, making real-world testing vital.

Interesting facts

Interesting Facts about (1-ethynylcyclohexyl) N-carbamoylcarbamate

(1-ethynylcyclohexyl) N-carbamoylcarbamate is a fascinating compound that attracts attention due to its unique structural and functional properties. Here are some engaging insights into this compound:

  • Structure and Composition: This compound features a cyclohexyl ring, which is known for its stability and rigidity, contributing positively to the overall chemical behavior of the molecule.
  • Functions in Chemistry: As a carbamate derivative, it is valuable in organic synthesis and medicinal chemistry, where carbamates are often utilized for their role in various biological activities.
  • Potential Applications: Researchers are exploring its potential use in pharmaceuticals, agrochemicals, and polymers. Its unique ethynyl group can lead to enhanced reactivity and selectivity in organic reactions.
  • Scientific Interest: Due to its distinctive functionalities, (1-ethynylcyclohexyl) N-carbamoylcarbamate serves as a pivotal subject in studies aimed at improving drug delivery mechanisms and developing novel therapeutic agents.
  • Environmental Considerations: As with many organic compounds, understanding the environmental impact and degradability of carbamate derivatives is critical, which can inform safer use and disposal methods.

In summary, (1-ethynylcyclohexyl) N-carbamoylcarbamate is not just another compound in organic chemistry; it holds potential for groundbreaking applications and research, making it an intriguing subject for both chemists and students alike.

Synonyms
Dolcental
ALLOPHANIC ACID, 1-ETHYNYLCYCLOHEXYL ESTER
Clocental
562-94-7
UX2C2JZD57
Carbamic acid, (aminocarbonyl)-, 1-ethynylcyclohexyl ester
1-Ethynylcyclohexyl allophanate
(1-ethynylcyclohexyl) N-carbamoylcarbamate
1-Aethinyl-cyclohexyl-allophanat-(1)
Cyclohexanol, 1-ethynyl-, allophanate
BRN 3316756
Docental
1-Aethinyl-cyclohexyl-allophanat-(1) [German]
UNII-UX2C2JZD57
4-06-00-00350 (Beilstein Handbook Reference)
DTXSID80204741
1-Ethynylcyclohexyl N-carbamoylcarbamate