CAS 89502-21-6
:3-Isothiazolecarboxylic acid, 4-(chlorosulfonyl)-, methyl ester
Description:
3-Isothiazolecarboxylic acid, 4-(chlorosulfonyl)-, methyl ester is a chemical compound characterized by its isothiazole ring structure, which contributes to its unique reactivity and properties. The presence of a chlorosulfonyl group enhances its electrophilic character, making it useful in various chemical reactions, particularly in the synthesis of more complex molecules. As a methyl ester, it exhibits typical ester characteristics, such as being relatively stable under standard conditions but hydrolyzing in the presence of water or strong bases. This compound is often utilized in organic synthesis and may have applications in agrochemicals or pharmaceuticals due to its potential biological activity. Its CAS number, 89502-21-6, allows for precise identification and cataloging in chemical databases. Safety considerations should be taken into account when handling this compound, as the chlorosulfonyl group can be reactive and may pose health risks if not managed properly. Overall, this compound exemplifies the diverse functionalities that can be derived from heterocyclic chemistry.
Formula:C5H4ClNO4S2
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Found 1 products.
Methyl 4-(chlorosulfonyl)-1,2-thiazole-3-carboxylate
CAS:<p>Versatile small molecule scaffold</p>Formula:C5H4ClNO4S2Purity:Min. 95%Molecular weight:241.7 g/mol
