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

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Identification
Molecular formula
C19H13BrN2O6S
CAS number
123456-78-9
IUPAC name
(2-nitrophenyl) N-[4-(4-bromophenyl)sulfonylphenyl]carbamate
State
State

At room temperature, the compound is typically found in a solid crystalline form. Care should be taken to prevent exposure to moisture or excessive light, which could affect its stability.

Melting point (Celsius)
205.30
Melting point (Kelvin)
478.45
Boiling point (Celsius)
512.50
Boiling point (Kelvin)
785.65
General information
Molecular weight
473.29g/mol
Molar mass
473.2900g/mol
Density
1.5423g/cm3
Appearence

The compound appears as a pale yellow crystalline powder. Its fine particulate form can make it prone to dispersion in air, resulting in potential inhalation hazards if not handled in a controlled environment.

Comment on solubility

Solubility of (2-nitrophenyl) N-[4-(4-bromophenyl)sulfonylphenyl]carbamate

The solubility of (2-nitrophenyl) N-[4-(4-bromophenyl)sulfonylphenyl]carbamate is influenced by several key factors. Understanding these aspects can provide valuable insights into its behavior in various solvents:

  • Nature of Solvents: This compound tends to be more soluble in organic solvents such as dimethyl sulfoxide (DMSO) and acetone, while showing limited solubility in water due to its complex structure.
  • Temperature Influence: Increased temperatures can promote greater solubility; hence, heating organic solvents can enhance the dissolution process of this compound.
  • Polarity Considerations: Since the compound features both polar and non-polar segments, its solubility is markedly affected by the polarity of the solvent used. It favors polar aprotic solvents.
  • pH Sensitivity: The solubility can vary with changes in pH, particularly if the compound undergoes protonation or deprotonation in response to the solution's acidity or alkalinity.

In summary, when evaluating the solubility of (2-nitrophenyl) N-[4-(4-bromophenyl)sulfonylphenyl]carbamate, it is essential to consider the solvent's polarity, the temperature, and the pH levels. As with many complex organic compounds, making informed choices about solvent and conditions will optimize dissolution and reactivity.

Interesting facts

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

(2-nitrophenyl) N-[4-(4-bromophenyl)sulfonylphenyl]carbamate is a fascinating compound, particularly due to its structural complexity and potential applications in both the pharmaceutical and agricultural fields.

Chemical Structure and Properties

The compound features a unique molecular architecture that includes:

  • Nitrophenyl group which is known for its electron-withdrawing properties, influencing the reactivity of the molecule.
  • A sulfonyl group that enhances solubility and stability, making it an intriguing candidate for various reactions.
  • A bromophenyl moiety that can play a significant role in pharmacological activities.

Applications

This compound is particularly noteworthy for its potential uses:

  • It may serve as a lead structure in the development of novel anti-inflammatory or antimicrobial agents.
  • Its sulfonyl functionality is a common feature in compounds exhibiting biological activity, ensuring that this molecule could be biologically relevant.
  • Due to its nitro group, it can undergo various chemical reactions that can lead to the synthesis of more complex compounds.

Research Significance

Studies focusing on this compound might explore:

  • The mechanisms through which the nitro and sulfonyl groups contribute to its biological activity.
  • The potential for this compound to act as a prodrug, where it is converted to an active form in the body.
  • Interactions with biological systems that could lead to new therapeutic avenues.

In conclusion, (2-nitrophenyl) N-[4-(4-bromophenyl)sulfonylphenyl]carbamate stands as a testament to the complexity of chemical compounds, providing a wealth of opportunities for research and application in various scientific fields. It illustrates the beauty of organic chemistry where simple modifications can yield significant functional variations in molecules.

Synonyms
BRN 3018088
CARBANILIC ACID, p-((p-BROMOPHENYL)SULFONYL)-, o-NITROPHENYL ESTER
o-Nitrophenyl p-((p-bromophenyl)sulfonyl)carbanilate
14304-70-2
p-((p-Bromophenyl)sulfonyl)carbanilic acid o-nitrophenyl ester
DTXSID00162298
DTXCID4084789