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Ethyl N-(7-oxocyclohepta-1,3,5-trien-1-yl)carbamate

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Identification
Molecular formula
C11H13NO3
CAS number
106721-15-9
IUPAC name
ethyl N-(7-oxocyclohepta-1,3,5-trien-1-yl)carbamate
State
State

At room temperature, ethyl N-(7-oxocyclohepta-1,3,5-trien-1-yl)carbamate is typically in a solid state. Its structured formation allows it to maintain integrity as a solid under standard conditions.

Melting point (Celsius)
180.00
Melting point (Kelvin)
453.15
Boiling point (Celsius)
295.00
Boiling point (Kelvin)
568.15
General information
Molecular weight
207.23g/mol
Molar mass
207.2310g/mol
Density
1.2000g/cm3
Appearence

Ethyl N-(7-oxocyclohepta-1,3,5-trien-1-yl)carbamate typically appears as a crystalline solid powder, which can range in color from white to a light yellow. It is important to note that its appearance might slightly vary depending on the purity of the sample.

Comment on solubility

Solubility of Ethyl N-(7-oxocyclohepta-1,3,5-trien-1-yl)carbamate

Ethyl N-(7-oxocyclohepta-1,3,5-trien-1-yl)carbamate is a compound that showcases intriguing solubility characteristics, largely influenced by its molecular structure and functional groups. Understanding its solubility can be essential in applications such as drug formulation and chemical synthesis. Here are some key points to consider:

  • Polarity: The presence of the carbamate functional group adds polar characteristics, which may enhance solubility in polar solvents such as water or alcohols.
  • Hydrophobic Regions: The cyclohepta-triene structure introduces hydrophobic components that can lead to decreased solubility in highly polar environments.
  • Temperature Dependency: Like many organic compounds, the solubility of this carbamate can vary with temperature, often increasing at elevated temperatures.
  • Solvent Compatibility: The compound may have better solubility in organic solvents such as dichloromethane or ethyl acetate due to the balance of polar and non-polar regions.

In conclusion, the solubility of ethyl N-(7-oxocyclohepta-1,3,5-trien-1-yl)carbamate presents a nuanced interplay between polar and non-polar attributes, highlighting the importance of solvent selection in achieving optimal dissolution. As with many chemical compounds, the context of usage will dictate the most effective solubility parameters.

Interesting facts

Interesting Facts about Ethyl N-(7-oxocyclohepta-1,3,5-trien-1-yl)carbamate

Ethyl N-(7-oxocyclohepta-1,3,5-trien-1-yl)carbamate is a fascinating compound with a diverse range of applications and properties that make it of interest to chemists and researchers alike. Here are several noteworthy aspects of this compound:

  • Structural Complexity: The presence of the cycloheptatriene ring system lends this compound a unique structural profile. Its intricate arrangement allows for interesting interactions with other molecular entities, facilitating various chemical reactions.
  • Reactivity: The ketone functional group present in the compound enhances its reactivity, making it a valuable intermediate in organic synthesis, particularly in the production of more complex molecules.
  • Potential Biological Activity: Compounds with similar structures often exhibit significant biological activities. Researchers are exploring its potential uses in drug discovery and development, possibly leading to novel therapeutics.
  • Chemical Significance: The combination of the ethyl carbamate moiety with the unique triene system may present innovative pathways for catalysis and the design of new materials.
  • Research Opportunities: Due to its unique structure and properties, ethyl N-(7-oxocyclohepta-1,3,5-trien-1-yl)carbamate offers rich opportunities for further research—both in understanding its reactivity and exploring its potential as a functional material.

This compound exemplifies how the interplay of structure and function in organic chemistry can lead to exciting discoveries and advancements. As we continue to investigate such compounds, we unlock new possibilities in the realms of science and technology. It reminds us of the essential role of creativity and innovation within the field of chemistry.

Synonyms
18188-87-9
N-(2-Troponyl)ethylurethan
1,3,5-CYCLOHEPTATRIENE-1-CARBAMIC ACID, 7-OXO-, ETHYL ESTER
BRN 2805187
7-Oxo-1,3,5-cycloheptatriene-1-carbamic acid ethyl ester
DTXSID00171209
DTXCID6093700
ethyl N-(7-oxocyclohepta-1,3,5-trien-1-yl)carbamate