Interesting facts
Interesting Facts about 1-Chloro-3-phenyl-benzene
1-Chloro-3-phenyl-benzene, commonly known as 3-Chloro-1-phenylbenzene, is a fascinating organic compound that draws interest for its unique structure and potential applications. Here are some compelling aspects to consider:
- Structural Diversity: This compound features a benzene ring substituted with a chlorine atom and another phenyl group. This structural arrangement lends it interesting reactivity and properties due to the electron-withdrawing effects of chlorine.
- Applications in Synthesis: It serves as an important intermediate in organic synthesis. Chemists often utilize it in the production of various pharmaceuticals, agrochemicals, and dyes.
- Pharmacological Potential: The chlorinated aromatic compounds are frequently studied for their potential biological activity. For example, many exhibit antibacterial and antifungal properties, making them subjects of interest in medicinal chemistry.
- Environmental Considerations: Like many chlorinated compounds, it is essential to consider its environmental impact. Understanding its degradation pathways and toxicity is crucial for ensuring safe handling and disposal.
- Interesting Reactions: 1-Chloro-3-phenyl-benzene can undergo various chemical reactions, such as nucleophilic substitution or electrophilic aromatic substitution, opening doors for further chemical modifications.
As stated by renowned chemist Sir Derek Barton, "The art of chemistry lies in bridging structure and reactivity." 1-Chloro-3-phenyl-benzene perfectly exemplifies this principle, showcasing how a simple substitution can lead to complex possibilities.
Overall, 1-chloro-3-phenyl-benzene is more than a mere compound; it's a gateway to understanding the principles of organic chemistry, with numerous implications for research and industry.
Synonyms
3-CHLOROBIPHENYL
2051-61-8
m-Chlorobiphenyl
3-Chloro-1,1'-biphenyl
1,1'-Biphenyl, 3-chloro-
3-Chlorodiphenyl
3-Monochlorobiphenyl
Biphenyl, 3-chloro-
3-Chlorbiphenyl
UNII-WLQ4633SJY
EINECS 218-126-1
PCB 2
WLQ4633SJY
3-monochloro-1,1'-biphenyl
DTXSID1040299
CHEBI:36716
DTXCID9020299
218-126-1
1-chloro-3-phenylbenzene
11104-28-2
PCB No 2
Arochlor 1221
PCB No. 2
3-PCB
1,1'-Biphenyl,3-chloro-
3-Chloro[1,1'-biphenyl]
PCB 2 (3-Chlorobiphenyl)
m-Chlorodiphenyl
3'-chlorobiphenyl
3-chloro-biphenyl
MFCD00013633
PCB No. 2 10 microg/mL in Isooctane
1-chloranyl-3-phenyl-benzene
SCHEMBL170231
PCB No 2, analytical standard
1,1'-Biphenyl, 3-monochloro-
NMWSKOLWZZWHPL-UHFFFAOYSA-
AKOS006229877
BS-21894
DB-028455
CS-0204909
NS00003633
A814631
Q27891531
InChI=1/C12H9Cl/c13-12-8-4-7-11(9-12)10-5-2-1-3-6-10/h1-9H
Solubility of 1-chloro-3-phenyl-benzene
1-chloro-3-phenyl-benzene, also known as para-chlorobenzylphenyl, exhibits interesting solubility characteristics that are important to understand in various chemical applications.
The solubility of 1-chloro-3-phenyl-benzene can be summarized as:
Moreover, as stated in some studies, "the presence of chlorine in the benzene ring impacts its solubility by enhancing intermolecular forces with solvents of similar polarity." This highlights the significance of molecular structure in determining solubility.
In conclusion, understanding the solubility of 1-chloro-3-phenyl-benzene is crucial for its use in chemical reactions and applications, particularly in organic synthesis where appropriate solvent selection is key.