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

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Identification
Molecular formula
C19H13BrN2O6S
CAS number
109004-70-0
IUPAC name
(4-nitrophenyl) N-[4-(4-bromophenyl)sulfonylphenyl]carbamate
State
State

At room temperature, this carbamate compound is solid. It is typically stored in powder form for use in various chemical applications including synthesis and research.

Melting point (Celsius)
167.00
Melting point (Kelvin)
440.15
Boiling point (Celsius)
433.00
Boiling point (Kelvin)
706.15
General information
Molecular weight
453.28g/mol
Molar mass
453.2340g/mol
Density
1.5800g/cm3
Appearence

This compound is a solid with a crystalline appearance and light yellow color, characteristic of nitroaromatic compounds. The presence of the nitro group also often leads to a pale to bright yellow hue, depending largely on the concentration and particle size of the compound.

Comment on solubility

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

The solubility of the compound (4-nitrophenyl) N-[4-(4-bromophenyl)sulfonylphenyl]carbamate can be influenced by a number of factors including its chemical structure, polarity, and the presence of functional groups. Here are some key points to consider:

  • Polarity: The presence of both nitro (–NO2) and sulfonyl (–SO2) groups typically increases the compound's polarity, suggesting that it may have better solubility in polar solvents such as water and methanol.
  • Hydrogen Bonding: The potential for hydrogen bond formation with solvents can enhance solubility. The carbamate functional group (–NH–COO–) might participate in such interactions.
  • Solvent Effects: It is often observed that the solubility increases in solvents with similar dielectric constants. Thus, testing in various organic solvents might yield differing degrees of solubility.

However, due to the presence of bulky bromophenyl and nitrophenyl groups, solubility could be limited in some organic solvents. Therefore, it is essential to conduct empirical experiments to determine precise solubility characteristics. As a final note, understanding solubility is crucial for its applications and effectiveness in various chemical processes.

Interesting facts

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

(4-nitrophenyl) N-[4-(4-bromophenyl)sulfonylphenyl]carbamate is a fascinating compound that represents the intersection of organic chemistry and medicinal applications. This compound, due to its unique structure and functional groups, serves as an important subject of study. Here are some notable aspects:

  • Pharmaceutical Relevance: The compound belongs to a class of molecules often explored for their potential as pharmaceuticals. Compounds like this are assessed for their abilities to interfere with biological processes, making them candidates for drug development.
  • Coordination with Biological Targets: Its structure allows for interactions with various biological targets, particularly enzymes crucial in different metabolic pathways, potentially leading to therapeutic effects.
  • Nitro and Bromine Groups: The presence of nitro groups introduces electron-withdrawing characteristics. In contrast, bromine substitutions can enhance lipophilicity, justifying their investigation in drug formulation.
  • Environmental Concerns: Compounds that feature halogens, such as bromine, can raise environmental concerns regarding their persistence and bioaccumulation. Hence, the study of their degradation pathways is essential.

This compound exemplifies the importance of functional group manipulation in achieving desired biological activities. As you delve deeper into the world of organic compounds, you might find yourself asking questions such as:

  1. What specific biological activities can this compound exhibit?
  2. How does the structural configuration influence its interactions with target molecules?
  3. In what ways can the synthesis of such compounds be improved or made more environmentally friendly?

Overall, (4-nitrophenyl) N-[4-(4-bromophenyl)sulfonylphenyl]carbamate represents a significant area of interest in both academic research and practical applications, showcasing the harmonious balance of chemical structure and biological function.

Synonyms
BRN 3018114
CARBANILIC ACID, p-((p-BROMOPHENYL)SULFONYL)-, p-NITROPHENYL ESTER
p-Nitrophenyl p-((p-bromophenyl)sulfonyl)carbanilate
14193-09-0
p-((p-Bromophenyl)sulfonyl)carbanilic acid p-nitrophenyl ester
DTXSID60161863
DTXCID5084354