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Nifenalol

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Identification
Molecular formula
C20H14N2O6
CAS number
69885-60-1
IUPAC name
4-(diphenylcarbamoyloxy)-3-nitro-benzoic acid
State
State

At room temperature, Nifenalol is in a solid state. Its crystalline solid form is stable under standard conditions.

Melting point (Celsius)
203.00
Melting point (Kelvin)
476.15
Boiling point (Celsius)
330.00
Boiling point (Kelvin)
603.15
General information
Molecular weight
377.36g/mol
Molar mass
377.3630g/mol
Density
1.4700g/cm3
Appearence

Nifenalol typically appears as a yellow crystalline solid. This characteristic yellow coloration can be attributed to the presence of the nitro functional group in its structure. The crystalline nature of the compound is due to its well-defined molecular structure allowing it to pack in a regular lattice.

Comment on solubility

Solubility of 4-(Diphenylcarbamoyloxy)-3-nitro-benzoic acid (C20H14N2O6)

Understanding the solubility of 4-(diphenylcarbamoyloxy)-3-nitro-benzoic acid provides insights into its potential applications and behavior in various solvents. This compound's unique structure influences its solubility characteristics in the following ways:

  • Polarity: Due to the presence of multiple functional groups, including a carboxylic acid moiety, this compound displays polar properties. As a result, it tends to have better solubility in polar solvents.
  • Solvent Compatibility: It may dissolve well in solvents such as dimethyl sulfoxide (DMSO) and ethanol, while showing limited solubility in nonpolar solvents like hexane.
  • Temperature Effects: Solubility can be influenced by temperature, with an increase in temperature often leading to a greater solubility in various solvents.
  • Hydrogen Bonding: The presence of hydrogen bond donors and acceptors in the structure may enhance solubility in polar protic solvents through strong interactions.

In summary, the solubility of 4-(diphenylcarbamoyloxy)-3-nitro-benzoic acid is primarily dictated by its polar nature and the specific properties of its surrounding solvent environment. Understanding these factors is crucial for its effective utilization in chemical synthesis and various applications.

Interesting facts

Discovering 4-(Diphenylcarbamoyloxy)-3-nitro-benzoic Acid

4-(Diphenylcarbamoyloxy)-3-nitro-benzoic acid is a compound that showcases the intricacies of organic chemistry, particularly in the realm of synthetic applications. Here are some fascinating insights:

  • Functional Versatility: This compound contains both a nitro and carbamoyloxy group, making it an important structure for further chemical transformations.
  • Applications in Research: It has been explored in various research contexts, especially in the development of artificially engineered materials and pharmacological agents.
  • Role in Medicinal Chemistry: The presence of nitro groups can enhance biological activity, making it a candidate for drugs targeting specific enzymes or receptors.

Moreover, the compound serves as a prime example of the interplay between nitrogen and oxygen functionalities in organic structures. Its synthesis often involves multi-step processes that not only enrich the student's understanding of reactivity but also highlight the importance of protecting groups in complex organic synthesis.

As one researcher aptly put it, "The beauty of organic chemistry lies in the details—each compound has a story, and 4-(diphenylcarbamoyloxy)-3-nitro-benzoic acid is a compelling chapter."

In the hands of talented chemists, compounds like this can lead to innovations in material science and pharmaceuticals, making them key players in developing advanced technologies.

Synonyms
10556-88-4
2-nitro-4-carboxyphenyl-N,N-diphenylcarbamate
2-Ncdc
Ncp-dpcm
4-((Diphenylcarbamoyl)oxy)-3-nitrobenzoic acid
4-(diphenylcarbamoyloxy)-3-nitrobenzoic acid
NCDC
DTXSID80147200
Benzoic acid, 4-(((diphenylamino)carbonyl)oxy)-3-nitro-
SCHEMBL5064947
DTXCID3069691
AKOS016845861
4-((Diphenylcarbamoyl)oxy)-3-nitrobenzoicacid
2-Nitro-4-carboxyphenyl-N,N-diphenyl carbamate
2-NITRO-4-CARBOXYPHENYL N,N-DIPHENYLCARBAMATE