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Piflufenidol (common name unavailable)

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Identification
Molecular formula
C27H21NO2
CAS number
128018-28-2
IUPAC name
2-anilino-1-(4-benzyloxyphenyl)-2-phenyl-ethanone
State
State

At room temperature, this compound exists as a solid. It is typically handled in a powdered form, due to its stability and characteristic formation.

Melting point (Celsius)
117.50
Melting point (Kelvin)
390.65
Boiling point (Celsius)
443.50
Boiling point (Kelvin)
716.65
General information
Molecular weight
363.45g/mol
Molar mass
363.4510g/mol
Density
1.2200g/cm3
Appearence

This compound usually appears as a white or pale yellow solid, often provided in crystalline form for chemical analysis and applications.

Comment on solubility

Solubility of 2-anilino-1-(4-benzyloxyphenyl)-2-phenyl-ethanone

The solubility of 2-anilino-1-(4-benzyloxyphenyl)-2-phenyl-ethanone in various solvents is quite intriguing, as it largely affects its applications in both synthesis and formulation processes. Generally, its solubility can be influenced by several factors:

  • Polar vs. Nonpolar Solvents: This compound may exhibit greater solubility in nonpolar solvents due to its large organic structure, which incorporates phenyl and benzyloxy groups.
  • Temperature Dependence: As with many organic compounds, increased temperatures can enhance solubility, allowing for better dissolution, which can be critical during reactions.
  • pH Influence: The presence of an amino group can lead to pH-dependent solubility, where acidic or basic conditions might impact ionization and, consequently, solubility.

In summary, while specific quantitative solubility data may vary, it is essential to consider solvent polarity, temperature, and pH when evaluating the solubility profile of 2-anilino-1-(4-benzyloxyphenyl)-2-phenyl-ethanone. Understanding these aspects will aid researchers and manufacturers in optimizing its use in practical applications.

Interesting facts

Exploring 2-anilino-1-(4-benzyloxyphenyl)-2-phenyl-ethanone

2-anilino-1-(4-benzyloxyphenyl)-2-phenyl-ethanone, often referred to for its complex structure and notable applications, is a fascinating compound that presents numerous points of interest for chemists and students alike.

Key Characteristics

  • Structure Complexity: The compound is comprised of multiple functional groups, making it an intriguing subject for structural studies. Its molecular architecture includes an aniline group, which contributes to its reactivity and an aromatic system.
  • Biological Activity: Initial studies suggest potential biological activities, possibly in the realm of medicinal chemistry. Compounds with such structures have been known to exhibit activities such as antitumor and antimicrobial properties.
  • Synthetic Applications: The compound may serve as a versatile intermediate in organic synthesis, opening pathways to a variety of derivatives that can be tailored for specific chemical reactions.

Chemical Significance

This compound is a compelling example of how modifying an aromatic system can affect chemical behavior and biological functionality. As chemists explore the myriad effects of molecular structure on properties, compounds like 2-anilino-1-(4-benzyloxyphenyl)-2-phenyl-ethanone serve as a bridge between theoretical study and practical application.

Research and Development Potential

The compound’s unique structure makes it a *prime candidate* for research in:

  • Pharmacology: Could uncover new drug candidates that influence cellular pathways.
  • Material Science: Possesses properties that may lend to the development of advanced materials.
  • Green Chemistry: Ongoing research could lead to more sustainable synthesis routes.

In conclusion, the exploration of 2-anilino-1-(4-benzyloxyphenyl)-2-phenyl-ethanone is a reminder of the intricate relationship between chemical structure and function. As we dive deeper into its study, we may unlock a wealth of knowledge that could have *significant implications* for both science and industry.

Synonyms
14293-15-3
BRN 2821281
alpha-Anilino-p-benzyloxyphenyl benzyl ketone
2-Anilino-4'-(benzyloxy)-2-phenylacetophenone
4'-(alpha-Anilinobenzyloxy)-2-phenylacetophenone
ACETOPHENONE, 2-ANILINO-4'-(BENZYLOXY)-2-PHENYL-
2-(PHENYLAMINO)-4'-(BENZYLOXY)-2-PHENYLACETOPHENONE
DTXSID20931685
2-Anilino-1-[4-(benzyloxy)phenyl]-2-phenylethan-1-one