Interesting facts
Interesting Facts about (4-aminophenyl)-phenyl-methanone
(4-aminophenyl)-phenyl-methanone, also known by its IUPAC name, is a fascinating compound with a variety of applications and characteristics that make it valuable in both research and industry.
Key Features
- Structural Significance: This compound contains an amine group attached to a phenyl ring, which makes it an aromatic amine. The presence of both an amine and a ketone group in the structure adds complexity and contributes to its reactivity.
- Versatile Intermediate: It serves as a crucial intermediate in the synthesis of various pharmaceuticals and agrochemicals. The ability to modify the phenyl groups allows chemists to develop new formulations with tailor-made properties.
- Potential Uses: The compound has potential as a precursor in the synthesis of dyes, resins, and biologically active molecules. Furthermore, some derivatives have shown promise in medicinal chemistry, particularly in anti-cancer and anti-inflammatory drug research.
Chemical Behavior
- Reactivity: The amine part of the compound participates in various chemical reactions, including nucleophilic substitutions and coupling reactions, which are essential in drug discovery.
- Hydrogen Bonding: The presence of the amine group enhances the capability to form hydrogen bonds, affecting solubility and interaction with biological targets.
The study of (4-aminophenyl)-phenyl-methanone is a prime example of how intricate structure can lead to diverse applications. As chemists continue to explore its properties, they discover more about its potential to influence fields ranging from pharmaceuticals to materials science. As one researcher aptly stated, “The beauty of chemistry lies in the surprises hidden within each molecule, waiting to be uncovered.”
Synonyms
4-Aminobenzophenone
1137-41-3
Methanone, (4-aminophenyl)phenyl-
Benzophenone, 4-amino-
p-Aminobenzophenone
p-Benzoylaniline
USAF A-233
NSC 7665
9VH7LQN5JE
EINECS 214-506-6
BRN 0389292
AI3-03267
NSC-7665
DTXSID8061557
4-14-00-00248 (Beilstein Handbook Reference)
DTXCID0033332
214-506-6
(4-aminophenyl)(phenyl)methanone
4-BENZOYLANILINE
444317-48-0
(4-aminophenyl)-phenylmethanone
MFCD00007895
CHEMBL314211
4-amino-benzophenone
4-Aminophenyl phenyl ketone
(4-aminophenyl)-phenyl-methanone
NSC7665
4-Benzoylbenzenamine
para-aminobenzophenone
aniline, 4-benzoyl-
UNII-9VH7LQN5JE
WLN: ZR DVR
Oprea1_489892
SCHEMBL49952
(4-Amino-phenyl)phenylmethanone
(4-Aminophenyl)phenyl-methanone
(4-Amino-phenyl)phenyl-methanone
(4-Amino-phenyl)-phenyl-methanone
BDBM50145839
AKOS009158785
FA71381
HY-W076903
s12116
AC-15859
DS-14627
SY048508
DB-027778
DB-344724
A1140
CS-0113883
NS00023696
EN300-67231
AJ-333/09219011
Q63399175
Z1069985914
Solubility of (4-aminophenyl)-phenyl-methanone
(4-aminophenyl)-phenyl-methanone, also known as 4-aminobenzophenone, exhibits interesting solubility properties that are essential for various applications in organic chemistry and material science.
In general, the solubility of this compound can be characterized as follows:
In summary, the solubility of (4-aminophenyl)-phenyl-methanone is not absolute and is influenced by several factors including solvent type, temperature, and pH. Therefore, for optimal use in reactions or formulations, it is essential to carefully select the conditions under which this compound is utilized.