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Pheneturide

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Identification
Molecular formula
C10H13N3O2
CAS number
90-69-7
IUPAC name
1-carbamoyl-3-(2-phenylethyl)urea
State
State

Solid at room temperature. It is typically found as a crystalline substance.

Melting point (Celsius)
142.00
Melting point (Kelvin)
415.15
Boiling point (Celsius)
327.00
Boiling point (Kelvin)
600.15
General information
Molecular weight
206.24g/mol
Molar mass
206.2390g/mol
Density
1.3062g/cm3
Appearence

Pheneturide is a crystalline solid. It is typically white or off-white in appearance, often forming fine crystalline powder.

Comment on solubility

Solubility of 1-carbamoyl-3-(2-phenylethyl)urea

1-carbamoyl-3-(2-phenylethyl)urea is a compound that exhibits interesting solubility characteristics. Understanding its solubility can be crucial for its application in various chemical processes. Here's an overview:

  • Polar Nature: Due to the presence of both urea and phenyl groups, the compound has a polar backbone which influences its interaction with solvents.
  • Solvent Compatibility:
    • It is more soluble in polar solvents such as water and methanol due to hydrogen bonding capability.
    • Less soluble in non-polar solvents like hexane, which do not stabilize its polar character.
  • Temperature Dependence: The solubility of 1-carbamoyl-3-(2-phenylethyl)urea can increase with temperature; thus, heating the solvent may enhance its solubility.

In summary, the solubility of 1-carbamoyl-3-(2-phenylethyl)urea is predominantly influenced by its polar functional groups and the choice of solvent. As the old adage goes, "like dissolves like," and this is evident in the behavior of this compound in various solvent environments.

Interesting facts

Interesting Facts About 1-Carbamoyl-3-(2-phenylethyl)urea

1-Carbamoyl-3-(2-phenylethyl)urea is a fascinating compound that sits at the crossroads of organic chemistry and medicinal applications. Here are some notable points regarding its characteristics:

  • Structural Significance: This compound features a unique combination of a carbamoyl group and a phenylethyl moiety, making it significant in the field of drug discovery. The presence of both functional groups contributes to its biological activity, which chemists often explore for therapeutic potentials.
  • Biological Activity: Studies have indicated that derivatives of urea compounds like 1-carbamoyl-3-(2-phenylethyl)urea can exhibit various pharmacological properties, including anti-inflammatory and analgesic effects. This has prompted research into its potential uses in treating different health conditions.
  • Synthesis Challenges: The synthesis of this compound can involve multiple steps and reaction conditions, making it a subject of interest for synthetic chemists who aim to develop more efficient methods for its production.
  • Research Applications: Scientists are keenly interested in exploring the compound's interaction at a molecular level, which could lead to advancements in medicinal chemistry and the development of new drugs.

In summary, 1-carbamoyl-3-(2-phenylethyl)urea is more than just a chemical entity; it represents a wealth of opportunities for research and application in various scientific fields. As the exploration of its properties continues, we may uncover even more about its potential impact on medicine and industry.

Synonyms
1-(2-Phenylethyl)biuret
1-Phenethylbiuret
BIURET, 1-PHENETHYL-
BRN 2809897
6774-15-8
DTXSID30218015
DTXCID50140506