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

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Identification
Molecular formula
C19H14N2O6S
CAS number
50211-17-1
IUPAC name
(4-nitrophenyl) N-[4-(benzenesulfonyl)phenyl]carbamate
State
State

At room temperature, the compound is in a solid state. It is typically stored and handled in solid form, exhibiting stability under standard laboratory conditions.

Melting point (Celsius)
201.00
Melting point (Kelvin)
474.15
Boiling point (Celsius)
525.50
Boiling point (Kelvin)
798.65
General information
Molecular weight
398.41g/mol
Molar mass
398.4090g/mol
Density
1.3823g/cm3
Appearence

The compound appears as a crystalline solid, characterized by its white to off-white color. The material exhibits typical crystalline properties such as sharp edges and facets. It may have a faint odor depending on purity and handling conditions.

Comment on solubility

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

The solubility of (4-nitrophenyl) N-[4-(benzenesulfonyl)phenyl]carbamate can be influenced by various factors including its molecular structure, temperature, and the solvent used. Generally, this compound's solubility can be described as follows:

  • Polar solvents: The presence of polar functional groups in the molecule suggests it may have better solubility in polar solvents such as water or alcohols.
  • Non-polar solvents: It is likely to have lower solubility in non-polar solvents, given its structural features that promote interactions with polar environments.
  • Temperature effect: Increasing the temperature often enhances solubility; thus, elevated temperatures may improve the dissolution rate of this compound in suitable solvents.

In conclusion, the solubility of (4-nitrophenyl) N-[4-(benzenesulfonyl)phenyl]carbamate is a complex interplay of its molecular characteristics and external conditions. To obtain precise solubility data, empirical studies in various solvents at controlled temperature would be highly beneficial.

Interesting facts

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

(4-nitrophenyl) N-[4-(benzenesulfonyl)phenyl]carbamate is a fascinating chemical compound known for its unique structure and potential applications in various fields. Here are some intriguing aspects of this compound:

  • Chemical Structure: This compound features a complex arrangement of functional groups, including a nitro group and a sulfonyl group. Its dual aromatic rings enhance the molecular stability and reactivity.
  • Applications in Research: As a derivative of carbamates, this compound is of interest in medicinal chemistry. Researchers investigate its role in drug development, particularly in designing inhibitors for specific biological targets.
  • Potential Biological Activity: Compounds like this one often exhibit neuroprotective and anti-inflammatory properties, making them valuable for creating new therapeutic agents.
  • Environmental Implications: The synthesis and degradation of such compounds raise questions in environmental chemistry, as some carbamate derivatives can impact ecosystems. Understanding their behavior is crucial.
  • Research Trends: There is a growing trend towards creating derivatives of carbamates with enhanced selectivity and activity. This compound serves as a benchmark for synthesizing novel agents with improved pharmacological profiles.

In summary, (4-nitrophenyl) N-[4-(benzenesulfonyl)phenyl]carbamate exemplifies the intricate relationship between structure and function in chemistry. The study of such compounds not only deepens our understanding of chemical interactions but also opens new avenues in drug discovery and environmental stewardship.

Synonyms
BRN 3015867
CARBANILIC ACID, p-(PHENYLSULFONYL)-, p-NITROPHENYL ESTER
p-(Phenylsulfonyl)carbanilic acid p-nitrophenyl ester
14257-87-5
DTXSID40162090
DTXCID8084581