Skip to main content

Phenylcarbamic acid

ADVERTISEMENT
Identification
Molecular formula
C7H7NO2
CAS number
103-79-7
IUPAC name
phenylcarbamic acid
State
State

At room temperature, phenylcarbamic acid is in solid state. It is stable under normal conditions of use, storage, and transport.

Melting point (Celsius)
52.00
Melting point (Kelvin)
325.15
Boiling point (Celsius)
212.00
Boiling point (Kelvin)
485.15
General information
Molecular weight
137.14g/mol
Molar mass
137.1350g/mol
Density
1.3500g/cm3
Appearence

Phenylcarbamic acid is a crystalline solid. It can appear as white or colorless crystals, depending on purity and specific crystal formation conditions. This compound is typically odorless but can have a slight chemical smell if impurities are present.

Comment on solubility

Solubility of Phenylcarbamic Acid

The solubility of phenylcarbamic acid (C7H8N2O) presents an intriguing case for study. Understanding its solubility characteristics can provide insights into its applications and behavior in various environments.

Phenylcarbamic acid is known to exhibit:

  • Moderate solubility in water: It typically shows limited solubility, which makes it less soluble compared to salts or highly polar compounds.
  • Solubility in organic solvents: It dissolves well in organic solvents like methanol and ethanol, showcasing its amphipathic nature.
  • Temperature dependence: Its solubility can vary with temperature, often increasing in warmer conditions.

A phrase that captures its essence is: 'like dissolves like.' This means that the polar nature of phenylcarbamic acid favors solubility in polar solvents, while its non-polar character may limit solubility in non-polar environments.

In summary, phenylcarbamic acid's solubility reflects its unique molecular structure and could be valuable for various chemical processes, highlighting the importance of understanding how different factors influence solubility.

Interesting facts

Interesting Facts about Phenylcarbamic Acid

Pheylcarbamic acid, also known as phenylurea, is a fascinating compound with numerous applications in both the scientific and industrial realms. Here are some key points that showcase its significance and versatility:

  • Therapeutic Potential: Phenylcarbamic acid derivatives have been researched for their potential as antidiabetic agents. They may work by influencing the metabolic pathways in a way that can help manage blood sugar levels.
  • Agriculture Use: Some derivatives are also employed in agriculture as herbicides. Their ability to interact with plant proteins has encouraged studies into eco-friendly pest management solutions.
  • Research Applications: Chemists use phenylcarbamic acid as a starting material for synthesizing various compounds, including pharmaceuticals and agrochemicals, thanks to its versatile reactivity.
  • Mechanism of Action: The compound acts mainly by inhibiting certain enzymes in biological systems. This makes it a valuable target for research into drug design.
  • Structural Similarity: The structure of phenylcarbamic acid is similar to that of urea, which contributes to its range of biological activities. This structural feature allows for modifications that can enhance its efficacy.

In summary, phenylcarbamic acid is not just a simple chemical entity; it plays a role in important fields like medicine and agriculture, and its study presents opportunities for further discoveries. As stated in a research article, "exploring phenylcarbamic acid derivatives could unveil new pathways in drug development." Emphasizing its importance, this compound continues to inspire both chemists and biologists in their quest for innovation.

Synonyms
Phenylcarbamic acid
Carbanilic acid
Carbanilsaeure
Phenylcarbamidsaeure
501-82-6
N-Hydroxy-N-phenylformamide
n-carboxyaniline
M19U56546G
31335-69-0
N-PHENYLCARBAMIC ACID
N-Phenylformohydroxamic acid
CCRIS 5135
UNII-M19U56546G
FORMOHYDROXAMIC ACID, N-PHENYL-
BRN 2081248
Carbamic acid, phenyl-
SCHEMBL7634
CARBANILIC ACID [MI]
CHEBI:52496
DTXSID30953378
0-15-00-00008 (Beilstein Handbook Reference)
Q27123473