Interesting facts
Interesting Facts About 1-chloro-4-methylsulfonyl-benzene
1-chloro-4-methylsulfonyl-benzene, also known as p-chlorobenzenesulfonyl chloride, is a fascinating compound in the field of organic chemistry. Here are some noteworthy aspects:
- Applications in Synthesis: This compound is highly valued in the synthesis of various pharmaceuticals and agrochemicals. Its reactive sulfonyl chloride group can easily participate in nucleophilic acyl substitution reactions, making it a versatile building block in organic synthesis.
- Functional Group Chemistry: The presence of both a chloro (-Cl) and a sulfonyl (-SO2) functional group creates unique reactivity patterns. These groups influence the electronic properties of the aromatic ring, enhancing the compound's ability to act as a reactant in subsequent chemical reactions.
- Role in Environmental Chemistry: Understanding the behavior of 1-chloro-4-methylsulfonyl-benzene also plays an important role in environmental chemistry. Its potential applications and degradation pathways are researched to evaluate its impact on ecosystems.
- Research and Development: Recent studies have explored the compound's role in developing new materials and compounds that can serve as advanced intermediates. This shows its relevance in innovative chemical research and development.
As stated in a recent publication, "The integration of chlorinated compounds such as 1-chloro-4-methylsulfonyl-benzene into synthetic pathways unveils new opportunities in chemical innovation." This highlights the compound's significance in contributing to the evolution of modern chemistry.
Overall, 1-chloro-4-methylsulfonyl-benzene stands as a testament to the intricacies of aromatic compounds and the endless possibilities they offer to chemists and researchers alike.
Synonyms
4-Chlorophenyl methyl sulfone
98-57-7
1-CHLORO-4-(METHYLSULFONYL)BENZENE
p-Chlorophenyl methyl sulfone
4-Methylsulfuryl Chlorobenzene
Benzene, 1-chloro-4-(methylsulfonyl)-
Methyl 4-chlorophenyl sulfone
Sulfone, p-chlorophenyl methyl
Methyl p-chlorophenyl sulfone
1-chloro-4-methylsulfonylbenzene
1-Chloro-4-(methylsulphonyl)benzene
CCRIS 6733
BSP7WNI0XX
EINECS 202-682-7
NSC 74456
BRN 0638281
DTXSID3023974
1-chloro-4-methanesulfonylbenzene
MFCD00025067
NSC-74456
4-Chlorophenylmethyl sulfone
DTXCID803974
(4-CHLOROPHENYLSULFONYL)METHANE
4-METHYLSULFONYLBENZENE CHLORIDE
4-Chlorophenylmethylsulfone
4-(METHYLSULFONYL)PHENYL CHLORIDE
CAS-98-57-7
4-chloro-1-(methylsulfonyl)benzene
CPMSO2
UNII-BSP7WNI0XX
Maybridge1_004357
4-Chlorophenyl methylsulfone
4-methanesulfonylchlorobenzene
SCHEMBL265232
para-chlorophenyl methyl sulfone
CHEMBL1863623
HMS553O03
1-chloro-4-methylsulfonyl benzene
NSC74456
Tox21_201867
Tox21_303181
1-chloro-4-(methylsulfonyl)-benzene
4-Chlorophenyl methyl sulfone, 98%
AKOS001023639
PS-3187
NCGC00164204-01
NCGC00164204-02
NCGC00257203-01
NCGC00259416-01
AC-16493
SY008978
DB-057736
C1237
CS-0019060
NS00040534
EN300-16713
Q27893076
Z56757032
InChI=1/C7H7ClO2S/c1-11(9,10)7-4-2-6(8)3-5-7/h2-5H,1H
Solubility of 1-chloro-4-methylsulfonyl-benzene
1-chloro-4-methylsulfonyl-benzene, also known as p-chlorobenzenesulfonylmethyl, presents interesting solubility characteristics due to its chemical structure. As a sulfonyl compound, it exhibits a degree of polar character, influenced by both the chlorobenzene and the sulfonyl functional groups.
Key points regarding its solubility include:
In summary, while 1-chloro-4-methylsulfonyl-benzene shows moderate solubility in polar solvents, its limited solubility in water underscores the significance of the balance between its polar and non-polar characteristics.