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Fenuron

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Identification
Molecular formula
C10H12N2O2
CAS number
101-42-8
IUPAC name
1-carbamoyl-3-(3-phenylpropyl)urea
State
State

Fenuron is typically in a solid state at room temperature.

Melting point (Celsius)
159.00
Melting point (Kelvin)
432.15
Boiling point (Celsius)
282.00
Boiling point (Kelvin)
555.15
General information
Molecular weight
180.22g/mol
Molar mass
180.2150g/mol
Density
1.2860g/cm3
Appearence

Fenuron is typically a white crystalline solid.

Comment on solubility

Solubility of 1-Carbamoyl-3-(3-phenylpropyl)urea

1-Carbamoyl-3-(3-phenylpropyl)urea exhibits unique solubility characteristics that may influence its practical applications. When considering the factors affecting its solubility, several key points can be noted:

  • Polarity: The presence of both carbamoyl and urea functional groups typically enhances solubility in polar solvents like water.
  • Hydrogen Bonding: This compound can participate in hydrogen bonding, which tends to increase solubility in aqueous environments.
  • Hydrophobic Interactions: The phenylpropyl moiety introduces non-polar characteristics, which could limit solubility in water but enhance it in organic solvents.
  • Solvent Specificity: The solubility may vary significantly depending on the specific solvent used. For instance, solubility might be higher in solvents like dimethyl sulfoxide (DMSO) or ethanol due to their ability to solvate both polar and non-polar regions.

In conclusion, while 1-carbamoyl-3-(3-phenylpropyl)urea is expected to be soluble in polar solvents due to its functional groups, its overall solubility will greatly depend on the solvent environment, including temperature and pH conditions. Therefore, practical evaluations should be conducted to determine solubility in specific applications.

Interesting facts

Interesting Facts about 1-Carbamoyl-3-(3-phenylpropyl)urea

1-Carbamoyl-3-(3-phenylpropyl)urea is a unique compound that sits at the intersection of medicinal chemistry and agricultural applications. Here are some intriguing aspects of this compound:

  • Versatile Applications: This compound has potential uses in agriculture, particularly as a herbicide or fungicide due to its ability to inhibit specific biological pathways in plants.
  • Pharmacological Interest: Researchers are exploring its effects in pharmaceutical settings, particularly for targeting enzyme systems in disease modulation.
  • Structural Features: The presence of the phenyl group enhances its interaction with biological targets, facilitating better binding affinity and specificity.
  • Urea Moiety: The urea functional group in this compound is known for its ability to form hydrogen bonds, which is crucial for its reactivity and interaction with other bioactive molecules.
  • Synthetic Pathways: The synthesis of this compound involves strategic steps to ensure the correct formation of its complex structure, shedding light on advanced organic synthesis techniques used in modern chemistry.

This fascinating compound not only showcases the versatility of urea derivatives but also highlights the importance of continuing research in expanding its applications across different fields of science.

Synonyms
1-(3-Phenylpropyl)biuret
BIURET, 1-(3-PHENYLPROPYL)-
6774-17-0
BRN 2655586
DTXSID50218017
DTXCID70140508
1-carbamoyl-3-(3-phenylpropyl)urea