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6-(Diethylcarbamoyl)cyclohex-3-ene-1-carboxylic acid

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Identification
Molecular formula
C13H21NO3
CAS number
40487-99-6
IUPAC name
6-(diethylcarbamoyl)cyclohex-3-ene-1-carboxylic acid
State
State

Solid at room temperature, typically existing as a crystalline powder.

Melting point (Celsius)
132.00
Melting point (Kelvin)
405.15
Boiling point (Celsius)
284.00
Boiling point (Kelvin)
557.15
General information
Molecular weight
239.31g/mol
Molar mass
239.3140g/mol
Density
1.2000g/cm3
Appearence

This compound typically presents as a white or off-white crystalline solid. The crystals are often powdery in form.

Comment on solubility

Solubility of 6-(diethylcarbamoyl)cyclohex-3-ene-1-carboxylic acid

The solubility of 6-(diethylcarbamoyl)cyclohex-3-ene-1-carboxylic acid can be influenced by several factors, primarily due to its molecular structure and functional groups. This compound features both an acidic carboxylic acid group and a diethylcarbamoyl moiety, which can contribute to its solubility in various solvents.

Factors Affecting Solubility

  • Polarity: The presence of the carboxylic acid functional group typically enhances solubility in polar solvents, such as water, due to hydrogen bonding capabilities.
  • Hydrophobic Character: The cyclohexene ring, along with the ethyl groups from the diethylcarbamoyl, can impart some hydrophobic characteristics, which may reduce solubility in strictly polar solvents.
  • Solvent Type: This compound may exhibit better solubility in organic solvents (e.g. ethanol, dimethyl sulfoxide) due to the overall non-polar aspects of the cyclohexene structure.

When assessing solubility, one might categorize the behavior of this compound as follows:

  1. In Water: Moderate solubility is expected due to the carboxylic acid group.
  2. In Organic Solvents: Likely higher solubility, especially in less polar organic solvents.

In summary, the solubility of 6-(diethylcarbamoyl)cyclohex-3-ene-1-carboxylic acid varies significantly based on solvent choice, reflecting a balance between hydrophilic and hydrophobic interactions. Understanding these traits is essential for practical applications and further chemical explorations.

Interesting facts

Interesting Facts about 6-(Diethylcarbamoyl)cyclohex-3-ene-1-carboxylic Acid

This intriguing compound, 6-(diethylcarbamoyl)cyclohex-3-ene-1-carboxylic acid, is a member of a fascinating class of organic compounds characterized by their unique structure and potential applications in medicinal chemistry.

Structural Significance

The compound features a cyclohexene ring that acts as a fundamental backbone, which affects its chemical reactivity and interactions. Here are a few key points:

  • Cyclic Structure: The cyclohexene ring contributes to the compound's unique reactivity, particularly in electrophilic addition reactions.
  • Amino Acid Derivative: The diethylcarbamoyl group attached enhances its properties, making this compound resemble certain amino acid structures, important in biochemistry.

Potential Applications

6-(Diethylcarbamoyl)cyclohex-3-ene-1-carboxylic acid has garnered attention for its potential applications:

  • Pharmaceuticals: Its unique structure makes it a potential candidate for drug design, particularly as an analgesic or anti-inflammatory agent.
  • Biological Studies: This compound may serve as a useful tool in studying enzyme mechanisms due to its structural characteristics.

Chemical Properties

In the realm of chemical properties, this compound is noteworthy for:

  • Reactivity: The presence of both carboxylic acid and amide functional groups provides diverse reactivity pathways.
  • Stability: Its structural framework enhances stability compared to more linear or branched molecules, making it an interesting subject for further investigation.

As a chemistry student or scientist, delving into the properties and applications of 6-(diethylcarbamoyl)cyclohex-3-ene-1-carboxylic acid opens doors to understanding complex reactions and potential new discoveries in the field of organic chemistry.

Synonyms
6-(diethylcarbamoyl)cyclohex-3-ene-1-carboxylic acid
131-64-6
DTXSID40274723
DTXCID60226183
NSC6279
CERAPP_64914
DTXSID00872269
NSC-6279
AKOS000128627
NS00046902
4-diethylcarbamoyl-1-cyclohexene-5-carboxylic acid
3-Cyclohexene-1-carboxylic acid, 6-(diethylcarbamoyl)-
3-Cyclohexene-1-carboxylic acid, 6-[(diethylamino)carbonyl]-