CAS 677304-75-5
:6-Bromo-1,2-benzisothiazole-3-carboxylic acid
Description:
6-Bromo-1,2-benzisothiazole-3-carboxylic acid is a heterocyclic compound characterized by the presence of a benzisothiazole ring system, which incorporates both sulfur and nitrogen atoms. This compound features a bromine substituent at the 6-position and a carboxylic acid functional group at the 3-position, contributing to its reactivity and potential applications in various chemical reactions. The presence of the carboxylic acid group enhances its solubility in polar solvents and allows for potential interactions in biological systems. The bromine atom can serve as a site for further substitution reactions, making it a versatile intermediate in organic synthesis. Additionally, compounds of this type may exhibit biological activity, including antimicrobial or antifungal properties, which can be explored in pharmaceutical research. Its unique structural features and functional groups make it a valuable compound in the development of new materials and drugs. As with many heterocycles, the stability and reactivity of 6-Bromo-1,2-benzisothiazole-3-carboxylic acid can be influenced by environmental conditions such as pH and temperature.
Formula:C8H4BrNO2S
InChI:InChI=1/C8H4BrNO2S/c9-4-1-2-5-6(3-4)13-10-7(5)8(11)12/h1-3H,(H,11,12)
SMILES:c1cc2c(cc1Br)snc2C(=O)O
Synonyms:- 6-Bromobenzo[d]isothiazole-3-carboxylic acid
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Found 3 products.
6-Bromo-1,2-benzisothiazole-3-carboxylic acid
CAS:Formula:C8H4BrNO2SPurity:97%Color and Shape:SolidMolecular weight:258.09196-Bromobenzo[d]isothiazole-3-carboxylic acid
CAS:6-Bromobenzo[d]isothiazole-3-carboxylic acidPurity:97%Molecular weight:258.09g/mol6-Bromobenzo[d]isothiazole-3-carboxylic acid
CAS:Formula:C8H4BrNO2SPurity:97%Color and Shape:SolidMolecular weight:258.09


