CAS 221446-00-0
:1,2-Benzisothiazole-5-carboxylic acid, 2,3-dihydro-3-oxo-, 1,1-dioxide
Description:
1,2-Benzisothiazole-5-carboxylic acid, 2,3-dihydro-3-oxo-, 1,1-dioxide, with CAS number 221446-00-0, is a heterocyclic compound characterized by its benzothiazole core, which incorporates both sulfur and nitrogen in its structure. This compound typically exhibits properties associated with its functional groups, including acidic characteristics due to the carboxylic acid moiety. The presence of the 1,1-dioxide indicates that it has two oxygen atoms bonded to the sulfur atom, which can influence its reactivity and solubility. Generally, compounds of this type may display biological activity, making them of interest in pharmaceutical and agrochemical research. They can also participate in various chemical reactions, such as nucleophilic substitutions or cycloadditions, due to the electron-withdrawing nature of the benzothiazole ring. Additionally, the compound's stability, solubility in organic solvents, and potential for forming complexes with metal ions are important characteristics that can affect its applications in different fields, including materials science and medicinal chemistry.
Formula:C8H5NO5S
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Found 1 products.
1,1,3-Trioxo-2,3-dihydro-1,2-benzothiazole-5-carboxylic acid
CAS:<p>1,1,3-Trioxo-2,3-dihydro-1,2-benzothiazole-5-carboxylic acid is a carboxylic acid that can be prepared by sulfonation of 1,1,3-trioxo-2,3-dihydrobenzthiazole with sulfur dioxide and hydrochloric acid. This compound has been used as a sweetener in the food industry. It is also used as a precursor for other compounds such as 2,2′-[1,4]oxazinane and 2-[(pyridinium methylsulfonyl)amino]-N-(pyridinium methylsulfonyl) acetamide. The decarboxylated form of this compound is an iron chelator that binds to ferric ion. This compound reacts with copper ions to give copper complexes like 1-[(pyridinium methyls</p>Formula:C8H5NO5SPurity:Min. 95%Molecular weight:227.2 g/mol
