Interesting facts
Interesting Facts about 3,4-Dichlorobenzenesulfonyl Chloride
3,4-Dichlorobenzenesulfonyl chloride is a fascinating chemical compound that belongs to the class of sulfonyl chlorides, which are known for their utility in organic synthesis. Here are some noteworthy aspects of this compound:
- Versatile Reagent: This compound is a highly effective reagent in synthetic chemistry. Its ability to introduce a sulfonyl group into organic molecules makes it useful for the preparation of sulfonamides and other sulfonated compounds.
- Applications in Pharmaceuticals: The introduction of the sulfonyl group has significant implications in medicinal chemistry, as many sulfonyl-derived compounds exhibit antibacterial, antifungal, and antiviral activities.
- Friedel-Crafts Reaction: 3,4-Dichlorobenzenesulfonyl chloride can participate in Friedel-Crafts acylation reactions, which are essential for forming carbon-carbon bonds in aromatic compounds, thereby expanding the diversity of potential chemical products.
- Environmental Considerations: As with many chlorinated compounds, its use raises environmental concerns. It is crucial to handle this compound with care to mitigate any potential environmental impact from chlorinated waste.
- Synthetic Pathways: This compound can be synthesized through various pathways, including the chlorination of benzenesulfonic acid followed by thionyl chloride treatment. These pathways highlight the interplay of different reactions in organic synthesis.
To quote renowned chemist and researcher Dr. Jane Doe, “The power of sulfonyl chlorides lies in their reactivity and ability to drive complex reactions in a single step.” This illustrates not only the utility of 3,4-Dichlorobenzenesulfonyl chloride but also its importance in advancing modern chemical practices.
In summary, 3,4-Dichlorobenzenesulfonyl chloride is not just a mere compound but a significant tool in the hands of chemists, aiding in the advancement of both organic synthesis and pharmaceutical development.
Synonyms
3,4-DICHLOROBENZENESULFONYL CHLORIDE
98-31-7
3,4-Dichlorobenzene-1-Sulfonyl Chloride
Benzenesulfonyl chloride, 3,4-dichloro-
3,4-Dichlorobenzenesulphonyl chloride
3,4-Dichlorophenylsulfonyl chloride
3,4-dichlorobenzenesulfonylchloride
3,4-dichloro-benzenesulfonyl chloride
AI3-19279
NSC 2651
EINECS 202-656-5
MFCD00041255
3,4-dichlorobenzene-sulfonyl chloride
DTXSID5059165
NSC-2651
3,4-dichloro benzene sulfonyl chloride
AX3AD43WDD
SCHEMBL18316
DTXCID8049048
NSC2651
3,4dichlorobenzenesulfonyl chloride
3,4 dichlorophenyl sulfonylchloride
3,4-dichlorobenzenesulphonylchloride
ALBB-001007
3,4-dichlorophenylsulphonyl chloride
Benzenesulfonyl chloride,4-dichloro-
BBL037536
STK502400
3,4-dichlorobenzene sulfonyl chloride
3.4-dichloro-benzenesulfonyl chloride
AKOS000264827
CS-W012711
BP-10474
PS-10908
3,4-dichlorobenzene sulfonic acid chloride
3,4-Dichlorobenzenesulfonyl chloride, 95%
DB-021856
D2990
NS00040530
EN300-17164
Z56896790
Solubility of 3,4-dichlorobenzenesulfonyl chloride
3,4-dichlorobenzenesulfonyl chloride is a relatively polar organic compound, which influences its solubility in various solvents. Understanding its solubility profile is important for practical applications and synthesis.
Solubility Characteristics:
When discussing the solubility of 3,4-dichlorobenzenesulfonyl chloride, it is crucial to highlight its interaction with solvents. According to solubility rules:
Understanding these dynamics is essential for chemists who aim to utilize this compound effectively in reactions and synthetic processes.