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

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Identification
Molecular formula
C19H14N2O6S
CAS number
34546-89-7
IUPAC name
(2-nitrophenyl) N-[4-(benzenesulfonyl)phenyl]carbamate
State
State

At room temperature, (2-nitrophenyl) N-[4-(benzenesulfonyl)phenyl]carbamate exists as a solid. This solid state is stable under standard conditions of temperature and pressure.

Melting point (Celsius)
153.50
Melting point (Kelvin)
426.65
Boiling point (Celsius)
450.00
Boiling point (Kelvin)
723.00
General information
Molecular weight
398.40g/mol
Molar mass
398.3940g/mol
Density
1.4300g/cm3
Appearence

The compound typically appears as a crystalline solid. The color can range from light yellow to off-white. The texture is usually powdery or granular, depending on purity and form.

Comment on solubility

Solubility of (2-nitrophenyl) N-[4-(benzenesulfonyl)phenyl]carbamate

The solubility of (2-nitrophenyl) N-[4-(benzenesulfonyl)phenyl]carbamate can be influenced by several factors due to its complex structure. Understanding its solubility properties is crucial for applications in various chemical processes and formulations.

Key Solubility Insights:

  • Polarity: Being an amide derivative, it may present moderate polarity, which can affect its solubility in polar solvents like water.
  • Solvent Compatibility: It is likely to be more soluble in organic solvents such as ethanol or dimethyl sulfoxide (DMSO) due to its aromatic components.
  • Influence of Functional Groups: The presence of both nitro and sulfonyl groups can enhance interactions with solvents, potentially improving solubility in specific contexts.
  • Solubility Dependence: Temperature fluctuations may significantly alter solubility; higher temperatures may lead to increased solubility in organic media.

In summary, while the precise solubility of (2-nitrophenyl) N-[4-(benzenesulfonyl)phenyl]carbamate is not definitively characterized, it is reasonable to expect that its solubility will vary depending on the solvent used, temperature, and overall environmental conditions. As such, further empirical studies would be beneficial for a comprehensive understanding.

Interesting facts

Interesting Facts about (2-nitrophenyl) N-[4-(benzenesulfonyl)phenyl]carbamate

(2-nitrophenyl) N-[4-(benzenesulfonyl)phenyl]carbamate is an intriguing compound that displays significant potential in various fields of chemistry and biology. Here are some notable points worth highlighting:

  • Structural Complexity: This compound showcases a complex structure featuring both nitro and sulfonyl functional groups, which contribute to its unique properties and reactivity.
  • Biological Activity: Carbamates, in general, have been studied for their potential therapeutic applications. The presence of the nitrophenyl and sulfonyl groups may enhance the biological activity, making it suitable for drug design.
  • Synthetic Utility: The synthesis of this compound may involve multiple steps, providing an excellent case study for students and researchers interested in organic synthesis techniques and reaction mechanisms.
  • Applications in Agrochemicals: Compounds with similar structures can serve as pesticides or herbicides, adding to their importance in agricultural chemistry.
  • Research Potential: Its novel structure makes it a subject of interest for ongoing research in medicinal chemistry, as scientists explore its capacity for inhibition of specific biological pathways.

As compounds like (2-nitrophenyl) N-[4-(benzenesulfonyl)phenyl]carbamate continue to be explored, they remind us of the intricate connections between chemistry and its applications in health, agriculture, and beyond. Indeed, in the words of a notable chemist, "Every molecule has a story to tell, waiting to be discovered."

Synonyms
BRN 3015803
CARBANILIC ACID, p-(PHENYLSULFONYL)-, o-NITROPHENYL ESTER
p-(Phenylsulfonyl)carbanilic acid o-nitrophenyl ester
14193-10-3
DTXSID20161864
DTXCID0084355