Interesting facts
Interesting Facts about (4-chlorophenyl)-phenyl-methanone
(4-chlorophenyl)-phenyl-methanone, commonly referred to as a derivative of benzophenone, is an intriguing compound in organic chemistry with various applications in the fields of material science and pharmaceuticals. Here are some engaging insights about this compound:
- Structural Diversity: The compound features an extensive structure involving multiple aromatic rings. This structure is known for its ability to contribute to the compound's unique chemical properties and reactivity.
- Applications: Due to its photostability, (4-chlorophenyl)-phenyl-methanone is often used in the formulation of sunscreens and photoinitators in polymer chemistry. Its capability to absorb UV radiation makes it valuable in protective coatings.
- Biological Relevance: Studies have shown that derivatives of this compound possess promising biological activities, including antibacterial and anticancer properties. This opens avenues for further research into its pharmacological applications.
- Synthetic Pathways: The synthesis of (4-chlorophenyl)-phenyl-methanone can be achieved through various methods, commonly involving Friedel-Crafts acylation reactions. This illustrates the versatility of electrophilic aromatic substitution reactions in organic synthesis.
- Environmental Considerations: Like many aromatic compounds, studies are being conducted to understand the environmental impact of (4-chlorophenyl)-phenyl-methanone. Investigating its degradation products and their potential toxicity is crucial for environmental safety.
In summary, (4-chlorophenyl)-phenyl-methanone is not just a simple aromatic ketone; it is a compound with potential applications across chemistry, biology, and materials science. Understanding its properties and functions can lead to innovations in various industrial and pharmaceutical processes. As stated by a renowned chemist, *“In the world of molecules, the potential for discovery is limitless.”*
Synonyms
4-CHLOROBENZOPHENONE
134-85-0
(4-Chlorophenyl)(phenyl)methanone
p-Chlorobenzophenone
Methanone, (4-chlorophenyl)phenyl-
p-CBP
(4-chlorophenyl)-phenylmethanone
Benzophenone, 4-chloro-
4-chloro benzophenone
para-Chlorobenzophenone
(4-chlorophenyl)phenylmethanone
4-Benzoylphenyl chloride
UNII-WIH1IZ728U
p-Chlorophenyl phenyl ketone
4-chlorophenyl phenyl ketone
WIH1IZ728U
MFCD00000622
DTXSID2051687
HSDB 2740
NSC 2872
NSC-2872
CLEMASTINE (M2)
EINECS 205-160-7
4-CBP
Cetirizine Impurity (4-Chlorobenzophenone)
AI3-00705
DTXCID5030242
PHENYL 4-CHLOROPHENYL KETONE
4-CHLOROBENZOPHENONE [USP-RS]
4-CHLOROPHENYL-PHENYL METHANONE
4-Chlorobenzophenone(Chunks or pellets or flake)
MECLOZINE DIHYDROCHLORIDE IMPURITY C [EP IMPURITY]
4-CHLOROBENZOPHENONE (USP-RS)
MECLOZINE DIHYDROCHLORIDE IMPURITY C (EP IMPURITY)
pChlorobenzophenone
Meclozine Hydrochloride Imp. C (EP); Meclozine Imp. C (EP); 4-Chlorobenzophenone; (4-Chlorophenyl)phenylmethanone; Meclozine Dihydrochloride Impurity C; Meclozine Impurity C
paraChlorobenzophenone
Benzophenone, 4chloro
4-Chlorobenzophenone, 99%
SCHEMBL50462
phenyl-(4-chlorophenyl)-ketone
Benzophenone, 4-chloro-(8CI)
CHEMBL3560455
Methanone, (4chlorophenyl)phenyl
NSC2872
CHEBI:167846
BCP27841
STR01449
Tox21_304009
(4-Chlorophenyl)(phenyl)methanone #
STL453116
AKOS000119405
CS-W004344
FC10726
PS-7925
NCGC00357224-01
AC-23664
CAS-134-85-0
DB-042255
NS00000626
EN300-20342
D77656
AH-034/32828041
Q27292660
Z104477824
4-Chlorobenzophenone, United States Pharmacopeia (USP) Reference Standard
205-160-7
Solubility of (4-chlorophenyl)-phenyl-methanone
The solubility of (4-chlorophenyl)-phenyl-methanone, also known as benzyl 4-chlorobenzophenone or simply 4-chlorobenzophenone, is an interesting topic for discussion among chemists.
This compound is largely characterized by its hydrocarbon framework which affects its interactions with solvents. Here are some key points regarding its solubility:
As a general rule, like dissolves in like, so:
Overall, the solubility of (4-chlorophenyl)-phenyl-methanone showcases the fascinating balance between its structural characteristics and the properties of solvent systems. As such, understanding these interactions is essential for applications in organic chemistry and materials science.