
CAS 29198-86-5
:3-(1,3-benzothiazol-2-yl)propanoate
Description:
3-(1,3-benzothiazol-2-yl)propanoate, with the CAS number 29198-86-5, is an organic compound characterized by its benzothiazole moiety, which contributes to its unique chemical properties. This substance typically appears as a solid or crystalline material and is soluble in organic solvents, reflecting its non-polar characteristics. The presence of the propanoate group indicates that it is an ester, which can influence its reactivity and interactions with other chemical species. The benzothiazole ring is known for its biological activity, often exhibiting antimicrobial and antifungal properties, making this compound of interest in pharmaceutical and agricultural applications. Additionally, the compound may participate in various chemical reactions, such as esterification and nucleophilic substitutions, due to the functional groups present. Its stability and reactivity can be influenced by environmental factors such as pH and temperature. Overall, 3-(1,3-benzothiazol-2-yl)propanoate is a versatile compound with potential applications in various fields, including medicinal chemistry and materials science.
Formula:C10H8NO2S
InChI:InChI=1/C10H9NO2S/c12-10(13)6-5-9-11-7-3-1-2-4-8(7)14-9/h1-4H,5-6H2,(H,12,13)/p-1
SMILES:c1ccc2c(c1)nc(CCC(=O)[O-])s2
Synonyms:- 2-Benzothiazolepropanoic Acid, Ion(1-)
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Found 3 products.
2-Benzothiazolepropanoic acid
CAS:Formula:C10H9NO2SPurity:95%Color and Shape:SolidMolecular weight:207.24903-(1,3-Benzothiazol-2-yl)propanoic acid
CAS:<p>3-(1,3-Benzothiazol-2-yl)propanoic acid</p>Purity:≥95%Color and Shape:SolidMolecular weight:207.25g/mol3-Benzothiazol-2-yl-propionic acid
CAS:Formula:C10H9NO2SPurity:95.0%Color and Shape:SolidMolecular weight:207.25


