Interesting facts
Exploring 1-(Benzenesulfonyl)-4-chloro-benzene
1-(Benzenesulfonyl)-4-chloro-benzene is a fascinating compound with diverse applications in the field of organic chemistry. Here are some intriguing aspects of this compound that highlight its significance:
- Sulfonyl Group: The presence of the benzenesulfonyl group makes this compound highly versatile, as it can engage in various chemical reactions, particularly in electrophilic aromatic substitution.
- Pharmaceutical Relevance: Compounds containing similar structures are often investigated for their potential use in pharmaceuticals, particularly as intermediates in drug synthesis. They may exhibit antimicrobial and anti-inflammatory properties.
- Functionalization: The chlorobenzene moiety provides a platform for further functionalization. Chemists can introduce different substituents through nucleophilic aromatic substitution, broadening the scope of its chemical transformations.
- Importance in Materials Science: This compound can be utilized in the design of polymeric materials and can act as a monomer for the preparation of sulfonate-containing polymers, contributing to advances in material technology.
As noted by chemist Paul Ehrlich, "The art of medicine consists of amusing the patient while nature cures the disease." Similarly, the art of organic synthesis often lies in creatively manipulating compounds like 1-(benzenesulfonyl)-4-chloro-benzene to innovate new materials and medicines.
In summary, the exploration of 1-(benzenesulfonyl)-4-chloro-benzene showcases the blend of chemistry and creativity, emphasizing the compound’s role in advancing both pharmaceutical and material sciences.
Synonyms
4-Chlorophenyl phenyl sulfone
80-00-2
SULPHENONE
Sulfenone
4-Chlorodiphenyl sulfone
Trifenson
1-Chloro-4-(phenylsulfonyl)benzene
Sulfenon
Benzene, 1-chloro-4-(phenylsulfonyl)-
p-Chlorophenyl phenyl sulfone
Compound R-242
Sulfone, p-chlorophenyl phenyl
p-Monochlorophenyl phenyl sulfone
p-Chlorophenyl phenyl sulphone
4-Chlorodiphenyl sulphone
4-Chlordifenylsulfon
R-242-B
Caswell No. 211D
ENT 17,941
1-(benzenesulfonyl)-4-chlorobenzene
4-Chlordifenylsulfon [Czech]
R 242
NSC 404335
HSDB 1544
R-242
EINECS 201-242-1
EPA Pesticide Chemical Code 060501
BRN 1819254
7NVM546U2M
DTXSID9042259
AI3-17941
SULPHENONE [MI]
SULPHENONE [HSDB]
NSC-404335
P-CHLOROPHENYL PHENYL
P-CHLORODIPHENYL SULFONE
DTXCID7022259
UNII-7NVM546U2M
Sulferone
4Chlordifenylsulfon
Compound R242
MFCD00007549
4-chlorodiphenylsulfone
4Chlorodiphenyl sulfone
4Chlorodiphenyl sulphone
WLN: WSR&R DG
pChlorophenyl phenyl sulfone
4chlorophenyl phenyl sulfone
pChlorophenyl phenyl sulphone
Sulfone, pchlorophenyl phenyl
SCHEMBL250144
4-Chlorophenyl phenyl sulphone
1Chloro4(phenylsulfonyl)benzene
pMonochlorophenyl phenyl sulfone
CHEMBL3188889
Benzene, 1chloro4(phenylsulfonyl)
R242B
Tox21_301666
NSC404335
AKOS003272997
4-Chlorophenyl phenyl sulfone, >=97%
CAS-80-00-2
USEPA/OPP Pesticide Code: 060510
NCGC00255932-01
DB-056398
HY-121688
CS-0083058
NS00021361
D89408
AE-562/40879364
Q27268626
Solubility of 1-(benzenesulfonyl)-4-chloro-benzene
1-(benzenesulfonyl)-4-chloro-benzene, known for its unique structure, presents interesting solubility characteristics. The solubility of this compound can be influenced by several factors:
However, it’s important to note that despite its potential solubility in some solvents, 1-(benzenesulfonyl)-4-chloro-benzene might have limited solubility in others like aliphatic hydrocarbons due to its relatively sophisticated aromatic structure.
In summary, while the solubility landscape for 1-(benzenesulfonyl)-4-chloro-benzene is defined by its **polar characteristics**, environmental factors such as solvent choice and temperature play critical roles in determining its solubility behavior.