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(3-nitrophenyl) N-[4-(benzenesulfonyl)phenyl]carbamate

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Identification
Molecular formula
C19H14N2O6S
CAS number
NULL
IUPAC name
(3-nitrophenyl) N-[4-(benzenesulfonyl)phenyl]carbamate
State
State

At room temperature, (3-nitrophenyl) N-[4-(benzenesulfonyl)phenyl]carbamate is a solid. It has a stable molecular structure retaining its form under standard conditions, typically requiring heating to induce phase change.

Melting point (Celsius)
182.50
Melting point (Kelvin)
455.65
Boiling point (Celsius)
458.50
Boiling point (Kelvin)
731.65
General information
Molecular weight
398.40g/mol
Molar mass
398.4040g/mol
Density
1.4250g/cm3
Appearence

(3-Nitrophenyl) N-[4-(benzenesulfonyl)phenyl]carbamate is typically a crystalline solid with a light yellow to pale brown color. The crystalline nature is due to the organized structure of its molecules, allowing it to form solid crystals at room temperature.

Comment on solubility

Solubility of (3-nitrophenyl) N-[4-(benzenesulfonyl)phenyl]carbamate

The solubility of (3-nitrophenyl) N-[4-(benzenesulfonyl)phenyl]carbamate can be described with several key points:

  • Overall solubility: This compound exhibits moderate solubility in common organic solvents such as acetone and ethanol, while its solubility in water is generally low.
  • Polarity: The presence of both nitro and sulfonyl functional groups contributes to its polar character; however, large hydrophobic phenyl groups decrease the overall solubility in polar solvents.
  • Temperature influence: Solubility can increase with temperature, a common trend for many organic compounds—making it more accessible in heated solutions.
  • pH effect: The pH of the solution can also impact solubility, especially if acidic or basic groups are involved in ionization.

As observed, the solubility behavior of this compound is highly dependent on the solvent used, the temperature of the solution, and the surrounding pH. While it is not highly soluble in water, its significant solubility in organic solvents allows for various potential applications in chemical processes and reactions.

Interesting facts

Interesting Facts about (3-nitrophenyl) N-[4-(benzenesulfonyl)phenyl]carbamate

(3-nitrophenyl) N-[4-(benzenesulfonyl)phenyl]carbamate is a fascinating compound that combines the properties of both nitro and sulfonyl functional groups. Here are some intriguing aspects that highlight its significance:

  • Diverse Applications: This compound is often studied for its potential applications in pharmaceuticals, particularly as a *prodrug* that can be activated in the body to produce therapeutic effects. Its unique structure allows for targeted drug delivery.
  • Analytical Chemistry: The presence of the nitro group makes this compound an excellent candidate for various analytical techniques, including UV-Vis spectroscopy and mass spectrometry. These techniques help in understanding its stability and degradation pathways.
  • Structural Insights: The arrangement of functional groups within the compound makes it a subject of interest for *crystallography* studies. Analyzing its crystal structure can reveal valuable information about molecular interactions and bonding.
  • Environmental Impact: Understanding the breakdown products of this compound is essential for assessing its environmental impact. Researchers are keen on determining how its degradation products behave in natural ecosystems.
  • Potential for Innovation: The unique attributes of this compound inspire ongoing research into novel derivatives that might enhance its efficacy and minimize side effects in drug formulations.

In summary, (3-nitrophenyl) N-[4-(benzenesulfonyl)phenyl]carbamate exemplifies the intricate relationship between structure and function in medicinal chemistry. As scientists continue to explore its properties, this compound promises to contribute significantly to advancements in both pharmaceutical sciences and environmental studies.

Synonyms
BRN 3015862
CARBANILIC ACID, p-(PHENYLSULFONYL)-, m-NITROPHENYL ESTER
p-(Phenylsulfonyl)carbanilic acid m-nitrophenyl ester
14193-11-4
DTXSID80161865
DTXCID5084356