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(2-nitrophenyl) N-[4-(4-chlorophenyl)sulfonylphenyl]carbamate

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Identification
Molecular formula
C19H13ClN2O6S
CAS number
25636-16-0
IUPAC name
(2-nitrophenyl) N-[4-(4-chlorophenyl)sulfonylphenyl]carbamate
State
State

This compound is typically in a solid state at room temperature.

Melting point (Celsius)
210.00
Melting point (Kelvin)
483.15
Boiling point (Celsius)
503.00
Boiling point (Kelvin)
776.15
General information
Molecular weight
434.86g/mol
Molar mass
434.8580g/mol
Density
1.4500g/cm3
Appearence

The compound appears as a yellow solid, typically in the form of crystalline powder.

Comment on solubility

Solubility Overview

The compound (2-nitrophenyl) N-[4-(4-chlorophenyl)sulfonylphenyl]carbamate presents interesting challenges regarding its solubility profile. Understanding its solubility is crucial for applications in chemical synthesis and pharmaceuticals.


Solubility Characteristics:

  • Polar vs. Non-polar: The presence of both nitro and sulfonyl groups suggests that this compound may exhibit polar characteristics, which could enhance its solubility in polar solvents.
  • Typical Solvents: Common solvents to consider for solubility studies include dimethyl sulfoxide (DMSO), methanol, and water, although the latter may be less effective due to the compound's potential hydrophobic areas.
  • Temperature Influence: It's often observed that solubility increases with higher temperatures; hence, conducting solubility tests at elevated temperatures may yield better insights into its behavior.
  • pH Sensitivity: Given the functional groups present, the solubility of this carbamate may vary significantly with changes in pH, making it worth exploring under different acidic or basic conditions.

In conclusion, while the exact solubility of (2-nitrophenyl) N-[4-(4-chlorophenyl)sulfonylphenyl]carbamate requires empirical testing for precise determination, the aforementioned factors will likely play a significant role in its solubility behavior in various environments.

Interesting facts

Interesting Facts about (2-nitrophenyl) N-[4-(4-chlorophenyl)sulfonylphenyl]carbamate

(2-nitrophenyl) N-[4-(4-chlorophenyl)sulfonylphenyl]carbamate is a fascinating compound with a variety of chemical and biological attributes. Here are some noteworthy points about this compound:

  • Dual Activity: This carbamate derivative showcases potential dual activity, which means it may serve both as a pesticide and a pharmaceutical agent, demonstrating flexibility in its application.
  • Nitrophenyl Group: The presence of the nitrophenyl moiety is significant, as nitro groups often contribute to increased bioactivity and are instrumental in cellular signaling processes.
  • Sulfonyl Functionality: The sulfonyl group (-SO2-) is known for its ability to enhance solubility and improve the compound's interaction with biological targets, making it a key player in drug design.
  • Chlorophenyl Component: The chlorophenyl substituent can affect the compound’s electronic properties and reactivity, influencing its overall stability and potency in applications.
  • Environmental Considerations: As with many synthetic compounds, understanding the environmental impact of (2-nitrophenyl) N-[4-(4-chlorophenyl)sulfonylphenyl]carbamate is crucial. Research is ongoing to evaluate its degradation pathways and toxicology.

This compound showcases a unique structure that could lead to breakthroughs in both agricultural chemistry and medicinal chemistry. As a chemistry student, one could appreciate how modifications to the core structure can lead to variations in biological activity—an exciting intersection of organic synthesis and ecological awareness.

In summary, (2-nitrophenyl) N-[4-(4-chlorophenyl)sulfonylphenyl]carbamate exemplifies the diverse roles that sophisticated organic compounds play in scientific innovation, inviting further exploration and research in multiple fields.

Synonyms
BRN 3018089
CARBANILIC ACID, p-((p-CHLOROPHENYL)SULFONYL)-, o-NITROPHENYL ESTER
14193-06-7
p-((p-Chlorophenyl)sulfonyl)carbanilic acid o-nitrophenyl ester
DTXSID80161860
N-(4-(4'-Chlorophenylsulfonyl)phenyl)-(o)-nitrophenyl-urethane [French]
N-(4-(4'-Chlorophenylsulfonyl)phenyl)-(o)-nitrophenyl-urethane
DTXCID0084351