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Fenuron

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Identification
Molecular formula
C10H13N2O
CAS number
101-42-8
IUPAC name
1,1-dimethyl-3-(p-tolyl)urea
State
State

At room temperature, fenuron is a solid. It maintains a stable crystalline form under standard conditions for temperature and pressure.

Melting point (Celsius)
148.00
Melting point (Kelvin)
421.00
Boiling point (Celsius)
379.20
Boiling point (Kelvin)
652.30
General information
Molecular weight
163.20g/mol
Molar mass
163.2020g/mol
Density
1.1565g/cm3
Appearence

Fenuron typically appears as a white solid crystalline powder. It is often supplied as a powder for use in various industrial applications, including as a herbicide.

Comment on solubility

Solubility of 1,1-Dimethyl-3-(p-tolyl)urea

1,1-Dimethyl-3-(p-tolyl)urea, with its complex structure, exhibits specific solubility characteristics that are important for its applications. This compound, which is a urea derivative, tends to have varying solubility in different solvents.

Key Solubility Aspects:

  • Solvent Compatibility: Generally soluble in polar solvents such as water and alcohols, reflecting its ability to form hydrogen bonds.
  • Hydrophobic Segment: The presence of the p-tolyl group adds a hydrophobic nature, which can impact solubility in non-polar solvents, resulting in lower solubility.
  • Temperature Dependence: Solubility may increase with temperature due to enhanced molecular motion, which facilitates interactions between solute and solvent.

In summary, 1,1-dimethyl-3-(p-tolyl)urea showcases a delicate balance between polar and non-polar characteristics, which significantly influences its solubility profile. Therefore, when utilizing or studying this compound, it is vital to consider these solubility factors for effective application.

Interesting facts

Interesting Facts about 1,1-Dimethyl-3-(p-Tolyl)urea

1,1-Dimethyl-3-(p-tolyl)urea is a fascinating compound that belongs to the class of ureas, which play a significant role in both organic chemistry and pharmaceuticals. Here are some intriguing highlights about this compound:

  • Chemical Structure: The structure of this molecule features a urea core with two methyl groups and a para-tolyl group attached. This combination results in unique chemical properties and biological activities.
  • Biological Significance: Compounds derived from urea have been widely studied for their potential pharmacological activities. Urea derivatives may exhibit various biological effects, including anti-inflammatory and antitumor properties.
  • Research Applications: 1,1-Dimethyl-3-(p-tolyl)urea can serve as a useful intermediate in the synthesis of more complex organic molecules, making it valuable in organic synthesis research.
  • Interaction with Enzymes: This compound has been investigated for its interaction with certain enzyme systems, contributing to our understanding of enzyme mechanisms and substrate specificity.
  • Synthesis Methods: There are several methods for synthesizing this compound, which can involve the reaction of isocyanates with substituted amines or other reagents, emphasizing the creativity involved in synthetic chemistry.

As with many urea derivatives, 1,1-dimethyl-3-(p-tolyl)urea represents a bridge between simple organic compounds and their complex interactions in biological systems. Understanding its properties and applications is pivotal for advancing both academic research and industrial applications.

Synonyms
7160-01-2
1,1-Dimethyl-3-(p-tolyl)urea
Urea, N,N-dimethyl-N'-(4-methylphenyl)-
DTXSID60221835
AI3-61362
N'-(4-METHYLPHENYL)-N,N-DIMETHYLUREA
DTXCID90144326
666-819-6
3,3-dimethyl-1-(4-methylphenyl)urea
N,N-dimethyl-N'-(4-methylphenyl)urea
1,1-dimethyl-3-(4-methylphenyl)urea
Urea, 1,1-dimethyl-3-p-tolyl-
MFCD00088385
SCHEMBL4770587
CHEMBL2271018
HMS1666H09
AKOS001325991
MS-1759
EN300-8092586
Z55293743