
CAS 889672-72-4
:2-chlorothiazol-5-ylboronic acid pinacol ester
Description:
2-Chlorothiazol-5-ylboronic acid pinacol ester is a chemical compound characterized by its boronic acid functionality, which is significant in various organic synthesis applications, particularly in Suzuki coupling reactions. The presence of the thiazole ring contributes to its heterocyclic nature, enhancing its reactivity and potential biological activity. The chlorothiazole moiety may impart specific electronic properties, influencing the compound's reactivity and interaction with other molecules. The pinacol ester group serves to stabilize the boronic acid, making it more suitable for storage and handling while retaining its reactivity in coupling reactions. This compound is typically used in medicinal chemistry and materials science, where its unique structural features can be exploited for the development of pharmaceuticals or advanced materials. Additionally, the compound's solubility and stability in various solvents can vary, which is essential for its application in synthetic protocols. Overall, 2-chlorothiazol-5-ylboronic acid pinacol ester is a versatile building block in organic synthesis, with potential implications in drug discovery and development.
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Found 4 products.
2-Chlorothiazole-5-boronic acid pinacol ester
CAS:Formula:C9H13BClNO2SPurity:98%Color and Shape:LiquidMolecular weight:245.53402-Chloro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiazole
CAS:2-Chloro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiazolePurity:98%Molecular weight:245.54g/mol(2-Chlorothiazol-5-yl)boronic acid pinacol ester
CAS:Formula:C9H13BClNO2SPurity:98%Color and Shape:LiquidMolecular weight:245.532-Chloro-5-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1,3-thiazole
CAS:<p>Versatile small molecule scaffold</p>Formula:C9H13BClNO2SPurity:Min. 95%Molecular weight:245.54 g/mol



