Introduction of CAS:2494-79-3 | 4-CHLORO-3-CHLOROSULFONYLBENZOIC ACID
Chlorobenzoic acids can undergo various chemical reactions. For example, photodecomposition of chlorobenzoic acids under ultraviolet irradiation can lead to the replacement of chlorine by hydroxyl and hydrogen, producing hydroxybenzoic acids and benzoic acid itself . This suggests that 4-Chloro-3-chlorosulfonylbenzoic acid may also be susceptible to similar photodecomposition reactions.
Specification of CAS:2494-79-3 | 4-CHLORO-3-CHLOROSULFONYLBENZOIC ACID
|
ITEMS |
SPECIFICATION |
|
Purity |
97% |
|
Density |
1.694±0.06 g/cm3(Predicted) |
|
Form |
Solid |
|
Color |
Pale Beige to Light Beige |
Research Application of CAS:2494-79-3 | 4-CHLORO-3-CHLOROSULFONYLBENZOIC ACID
Photodecomposition Applications
4-Chloro-3-chlorosulfonylbenzoic acid is involved in photodecomposition studies. Ultraviolet irradiation of chlorobenzoic acids leads to the replacement of chlorine with hydroxyl and hydrogen, producing hydroxybenzoic acids and benzoic acid. Specifically, the 4-chloro isomer can convert to benzoic acid with a high conversion rate (Crosby & Leitis, 1969).
Synthesis of Heterocyclic Compounds
4-Chloro-3-chlorosulfonylbenzoic acid acts as a building block in the synthesis of various heterocyclic scaffolds. Its derivatives are useful in preparing substituted nitrogenous heterocycles with significant importance in drug discovery (Křupková et al., 2013).
Dibenzo-condensed Oxathiazepinecarboxylic Acid Synthesis
This compound is used in the synthesis of a new dibenzo-condensed oxathiazepinecarboxylic acid, starting from methyl ester of 2,4-dichloro-5-chlorosulfonylbenzoic acid. Its derivatives have various applications in chemical synthesis (Bychenkov et al., 2009).
Role in Carbonic Anhydrase Inhibition
4-Chloro-3-chlorosulfonylbenzoic acid is involved in the synthesis of primary sulfonamides which inhibit human carbonic anhydrases. This has potential therapeutic relevance (Sapegin et al., 2018).
Catalysis in Synthesis Reactions
It is used as a catalyst in the synthesis of benzimidazoles, demonstrating practicality and efficiency in chemical synthesis processes (Shitole et al., 2016).
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