The chemical substance known as (2E)-4-(1,1-Dioxido-3-oxo-1,2-benzisothiazol-2(3H)-yl)but-2-enoic acid, with the CAS number 10295-14-4, is characterized by its unique structural features that include a butenoic acid moiety and a benzisothiazole derivative. This compound typically exhibits properties associated with both organic acids and heterocyclic compounds. The presence of the dioxido and keto functional groups suggests potential reactivity, particularly in nucleophilic addition or substitution reactions. Its benzisothiazole core may impart biological activity, making it of interest in pharmaceutical research. The compound is likely to be soluble in polar solvents due to the presence of the carboxylic acid group, while its aromatic structure may contribute to hydrophobic interactions. Additionally, the geometric configuration indicated by the "(2E)" designation suggests a specific trans arrangement of substituents around the double bond, which can influence its reactivity and interaction with biological targets. Overall, this compound's unique structure and functional groups position it as a potentially valuable entity in various chemical and biological applications.

(2E)-4-(1,1-Dioxido-3-oxo-1,2-benzisothiazol-2(3H)-yl)but-2-enoic acid

10295-14-4: The chemical substance known as (2E)-4-(1,1-Dioxido-3-oxo-1,2-benzisothiazol-2(3H)-yl)but-2-enoic acid, with the CAS number 10295-14-4, is characterized by its unique structural features that include a butenoic acid moiety and a benzisothiazole derivative. This compound typically exhibits properties associated with both organic acids and heterocyclic compounds. The presence of the dioxido and keto functional groups suggests potential reactivity, particularly in nucleophilic addition or substitution reactions. Its benzisothiazole core may impart biological activity, making it of interest in pharmaceutical research. The compound is likely to be soluble in polar solvents due to the presence of the carboxylic acid group, while its aromatic structure may contribute to hydrophobic interactions. Additionally, the geometric configuration indicated by the "(2E)" designation suggests a specific trans arrangement of substituents around the double bond, which can influence its reactivity and interaction with biological targets. Overall, this compound's unique structure and functional groups position it as a potentially valuable entity in various chemical and biological applications.

CAS 10295-14-4

(2E)-4-(1,1-Dioxido-3-oxo-1,2-benzisothiazol-2(3H)-yl)but-2-enoic acid

4-(1,1-Dioxido-3-oxo-1,2-benzisothiazol-2(3H)-yl)but-2-enoic acid

Ref: 10-F512013