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(3-nitrophenyl) N-[4-(4-bromophenyl)sulfonylphenyl]carbamate

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Identification
Molecular formula
C19H13BrN2O6S
CAS number
854056-07-0
IUPAC name
(3-nitrophenyl) N-[4-(4-bromophenyl)sulfonylphenyl]carbamate
State
State

In its pure form at room temperature, this compound is typically a solid. It is not volatile and remains stable under standard laboratory conditions, although it should be handled with care as it may pose chemical hazards.

Melting point (Celsius)
218.20
Melting point (Kelvin)
491.35
Boiling point (Celsius)
572.80
Boiling point (Kelvin)
846.00
General information
Molecular weight
468.28g/mol
Molar mass
468.2830g/mol
Density
1.6710g/cm3
Appearence

This compound typically appears as a crystalline solid. The color can range from pale yellow to light brown, depending on purity and specific conditions of crystallization.

Comment on solubility

Solubility of (3-nitrophenyl) N-[4-(4-bromophenyl)sulfonylphenyl]carbamate

The solubility of (3-nitrophenyl) N-[4-(4-bromophenyl)sulfonylphenyl]carbamate is influenced by its complex structure, which combines both aromatic and polar functional groups. When considering its solubility, several factors come into play:

  • Polarity: The presence of the sulfonyl group can increase the polarity of the molecule, potentially enhancing solubility in polar solvents.
  • Aromatic interactions: The extensive aromatic character may lead to aggregation in organic solvents, affecting overall solubility.
  • Hydrogen bonding: The carbamate functional group can participate in hydrogen bonding, making it more soluble in hydrogen-bonding solvents.
  • Temperature effect: Like many organic compounds, solubility can increase with temperature, thus higher temperatures might enhance its solubility in chosen solvents.

In summary, while (3-nitrophenyl) N-[4-(4-bromophenyl)sulfonylphenyl]carbamate may exhibit solubility in specific organic solvents, its behavior can vary significantly based on the solvent's properties. It is critical to conduct experiments to accurately determine solubility values, as this compound's intricate interactions can yield varying results. In the words of chemists, “The right solvent can mean the difference between a well-dissolved compound and one that remains intractable.”

Interesting facts

Interesting Facts about (3-nitrophenyl) N-[4-(4-bromophenyl)sulfonylphenyl]carbamate

(3-nitrophenyl) N-[4-(4-bromophenyl)sulfonylphenyl]carbamate is a fascinating compound with a variety of noteworthy characteristics that capture the interest of chemists and researchers alike. Below are some intriguing aspects of this compound:

  • Versatile Applications: This compound is particularly significant in the field of medicinal chemistry. Its structural features make it a promising candidate for developing pharmaceuticals, especially in the treatment of diseases impacted by enzyme inhibition.
  • Structural Complexity: The presence of both nitro and bromophenyl moieties in its structure enhances its reactivity and opens up avenues for further chemical reactions, making it an interesting subject for synthetic studies.
  • Biological Activity: Compounds similar to this one often exhibit noteworthy biological activities, such as anti-inflammatory or antimicrobial properties, which have been subjects of intense research in the quest for new therapeutic agents.
  • Environmental Consideration: Understanding the behavior of such compounds in various environments is crucial. Researching their degradation paths can lead to insights into their safe usage and disposal, thus aligning with green chemistry principles.
  • Intriguing Chemical Interactions: The sulfonamide group present in this compound may promote specific interactions with biological targets, elucidating their mechanism of action and paving the way for the design of selective inhibitors in future pharmacological research.

“The brilliance of chemistry lies in our ability to understand and manipulate the intricacies of molecules.” This saying resonates well with the study of (3-nitrophenyl) N-[4-(4-bromophenyl)sulfonylphenyl]carbamate, as it exemplifies the profound impact of chemistry on health, environment, and technology.

Overall, this compound’s structural diversity and potential applications underscore its importance in both theoretical studies and practical applications within the chemical sciences.

Synonyms
BRN 3018103
CARBANILIC ACID, p-((p-BROMOPHENYL)SULFONYL)-, m-NITROPHENYL ESTER
m-Nitrophenyl p-((p-bromophenyl)sulfonyl)carbanilate
14193-08-9
p-((p-Bromophenyl)sulfonyl)carbanilic acid m-nitrophenyl ester
DTXSID00161862
DTXCID0084353