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1-methyl-3-phenylurea

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Identification
Molecular formula
C8H10N2O
CAS number
622-63-9
IUPAC name
1-methyl-3-phenyl-urea
State
State

1-Methyl-3-phenylurea is typically found in a solid state at room temperature.

Melting point (Celsius)
128.00
Melting point (Kelvin)
401.15
Boiling point (Celsius)
196.00
Boiling point (Kelvin)
469.15
General information
Molecular weight
150.17g/mol
Molar mass
150.1740g/mol
Density
1.1785g/cm3
Appearence

1-Methyl-3-phenylurea is a white to off-white crystalline solid.

Comment on solubility

Solubility of 1-methyl-3-phenyl-urea

1-methyl-3-phenyl-urea, a compound with diverse applications in various fields, exhibits moderate solubility characteristics that are noteworthy:

  • Solvent Compatibility: This compound is generally soluble in polar organic solvents, such as ethanol and dimethyl sulfoxide (DMSO). However, its solubility may decrease significantly in non-polar solvents.
  • Water Solubility: The solubility of 1-methyl-3-phenyl-urea in water is limited. This presents challenges for applications requiring aqueous solutions.
  • Temperature Effects: Like many organic compounds, the solubility can be affected by temperature; typically, increased temperatures can enhance solubility in organic solvents.

It is important to note that solubility is influenced by various factors, including:

  • Molecular Structure: The presence of a phenyl group can reduce polarity, affecting the compound's interaction with solvents.
  • pH Levels: Changes in pH can alter the ionization state of the compound, impacting its solubility in water.

In summary, while 1-methyl-3-phenyl-urea demonstrates moderate solubility in certain polar organic solvents, its limited solubility in water restricts its use in aqueous environments. Understanding these solubility properties is crucial for optimizing its applications.

Interesting facts

Interesting Facts about 1-methyl-3-phenyl-urea

1-methyl-3-phenyl-urea is a fascinating organic compound that serves as a valuable building block in synthetic chemistry. This compound features two distinct functional groups that aid in its reactivity and compatibility with various chemical reactions.

Key Attributes

  • Versatile Reactivity: The urea functional group in this compound enhances its reactivity. It can participate in diverse reactions such as nucleophilic substitutions and condensation reactions.
  • Role in Pharmaceuticals: Compounds of similar structure are often investigated for their potential pharmaceutical applications, including anti-cancer and anti-inflammatory properties.
  • Intermediate in Synthesis: This compound may act as an intermediate in the synthesis of more complex organic molecules, showcasing the importance of ureas in organic synthesis.

Applications

1-methyl-3-phenyl-urea contributes to various sectors, particularly in:

  • Agriculture: Urea derivatives have been explored for their potential use in agrochemicals.
  • Materials Science: These compounds are also evaluated for their role in the development of polymers and coatings.

Conclusion

As a compound with wide-ranging implications, 1-methyl-3-phenyl-urea exemplifies how simple organic structures can lead to significant advancements in multiple fields of chemistry and material science. Understanding such compounds is crucial for future innovations and applications.

Synonyms
1-Methyl-3-phenylurea
Defenuron
N-Methyl-N'-phenylurea
N-Phenyl-N'-methylurea
IPO 4328
CCRIS 2709
NSC 10989
NSC-10989
BRN 0742887
UNII-11YB479454
11YB479454
DTXSID1074416
4-12-00-00734 (Beilstein Handbook Reference)
IPO-4328
DTXCID7032555
622-469-6
sqbhgdsdvwcphn-uhfffaoysa-n
1007-36-9
Urea, N-methyl-N'-phenyl-
Urea, 1-methyl-3-phenyl-
1-methyl-3-phenyl urea
fenuron-monodemethyl
NSC10989
MFCD00014855
3-methyl-1-phenylurea
1-Methyl-3-phenyl-urea
SCHEMBL714237
CHEMBL584381
N-Methyl-N'-phenylurea compound
CHEBI:157705
AKOS005231955
NCI60_000241
CS-0112589
C22322
D77088
Q27251351
Z55293754