Interesting facts
Exploring (4-hydroxyphenyl)-phenyl-methanone
(4-hydroxyphenyl)-phenyl-methanone, often referred to in the realm of organic chemistry, is a fascinating compound for a variety of reasons. This compound features a unique structure that combines both hydroxyl and carbonyl functionalities, leading to interesting properties and applications. Below are some compelling facts about this molecule:
- Versatile Intermediary: This compound acts as an important intermediary in the synthesis of various pharmaceuticals and agrochemicals, making it a valuable asset in the chemical industry.
- Antioxidant Properties: Studies have shown that compounds like (4-hydroxyphenyl)-phenyl-methanone can exhibit significant antioxidant activities, which help in protecting cells from oxidative stress.
- Photochemical Reactions: This compound is known to participate in photochemical reactions, making it relevant in the field of photochemistry where light-induced processes are studied.
- Biological Activity: Research indicates that derivatives of this compound may possess potential biological activities, including anti-cancer properties, which are of great interest to medicinal chemists.
- Structure-Activity Relationship (SAR): Understanding the structure of (4-hydroxyphenyl)-phenyl-methanone allows chemists to make informed modifications to enhance its effectiveness or reduce side effects in therapeutic applications.
Overall, (4-hydroxyphenyl)-phenyl-methanone is a noteworthy compound that exemplifies the complexity and utility found within organic chemistry. Its diverse range of applications, combined with the intriguing possibilities for future research, make it a subject of great interest in both academic and industrial contexts.
Synonyms
4-Hydroxybenzophenone
1137-42-4
4-Benzoylphenol
(4-Hydroxyphenyl)(phenyl)methanone
Methanone, (4-hydroxyphenyl)phenyl-
p-Benzoylphenol
P-HYDROXYBENZOPHENONE
Benzophenone, 4-hydroxy-
(4-Hydroxyphenyl)phenylmethanone
4'-Hydroxybenzophenone
UNII-04R2LWS0MS
NSC 1887
EINECS 214-507-1
04R2LWS0MS
DTXSID5036684
AI3-00862
(4-hydroxyphenyl)-phenyl-methanone
NSC-1887
DTXCID3016684
para-hydroxybenzophenone
Benzophenone, 4-hydroxy-(6CI,7CI,8CI)
214-507-1
inchi=1/c13h10o2/c14-12-8-6-11(7-9-12)13(15)10-4-2-1-3-5-10/h1-9,14
npfyzdndjhzqky-uhfffaoysa-n
(4-hydroxyphenyl)-phenylmethanone
4-HYDROXY-BENZOPHENONE
MFCD00002355
CHEMBL194487
CHEBI:34421
4-hydroxyphenyl phenyl ketone
(4-hydroxyphenyl)phenyl-methanone
4-hydroxy-benzphenone
4-hydroxylbenzophenone
4-Hydroxy benzophenone
(4-HYDROXY-PHENYL)-PHENYLMETHANONE
4-HYDROXYBENZOPHONE
4-Hydroxybenzophenone, 98%
BIDD:ER0013
SCHEMBL124916
NSC1887
Tox21_201229
(4-Hydroxy-phenyl)-phenyl-methanone
BDBM50410491
N-(4-Hydroxylphenyl)-N'-phenylurea
STK045122
(4-Hydroxyphenyl)(phenyl)methanone #
AKOS000119744
1-(4-Hydroxyphenyl)-1-phenylmethanone
CS-W015653
FH24312
HY-W014937
PS-8242
NCGC00248965-01
NCGC00248965-02
NCGC00258781-01
PD065561
CAS-1137-42-4
DB-041182
DB-295371
H0222
NS00001331
EN300-21521
F11203
AB00376867-03
Q27116055
F0001-0279
Z104500636
(4-Hydroxyphenyl)phenyl-methanone;1-(4-Hydroxyphenyl)-1-phenylmethanone;4-Benzoylphenol
Solubility of (4-hydroxyphenyl)-phenyl-methanone
(4-hydroxyphenyl)-phenyl-methanone, also known as a derivative of ketone, exhibits unique solubility characteristics that can be summarized as follows:
In summary, while (4-hydroxyphenyl)-phenyl-methanone is more compatible with organic solvents, its limited solubility in polar environments can pose challenges in specific applications. As with many organic compounds, solubility is affected not only by the nature of the solvent but also by external factors like temperature and molecular structure.