CAS 1125409-85-9
:ethyl 5-broMo-2-chlorothiazole-4-carboxylate
Description:
Ethyl 5-bromo-2-chlorothiazole-4-carboxylate is a chemical compound characterized by its thiazole ring, which is a five-membered heterocyclic structure containing both sulfur and nitrogen. The presence of bromine and chlorine substituents on the thiazole ring contributes to its reactivity and potential applications in various chemical reactions. The ethyl ester functional group enhances its solubility in organic solvents, making it useful in synthetic organic chemistry. This compound may exhibit biological activity, which is often explored in pharmaceutical research, particularly in the development of agrochemicals or medicinal compounds. Its molecular structure suggests potential interactions with biological targets, and the halogen substituents can influence its pharmacokinetic properties. Additionally, the compound's synthesis typically involves standard organic reactions, such as halogenation and esterification. Overall, ethyl 5-bromo-2-chlorothiazole-4-carboxylate is a versatile building block in organic synthesis with potential applications in medicinal chemistry and material science.
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Found 4 products.
Ethyl 5-bromo-2-chlorothiazole-4-carboxylate
CAS:Formula:C6H5BrClNO2SPurity:95%Color and Shape:SolidMolecular weight:270.5314Ethyl 5-bromo-2-chlorothiazole-4-carboxylate
CAS:Ethyl 5-bromo-2-chlorothiazole-4-carboxylatePurity:95%Molecular weight:270.53g/molEthyl 5-bromo-2-chlorothiazole-4-carboxylate
CAS:Formula:C6H5BrClNO2SPurity:95%Molecular weight:270.53Ethyl 5-bromo-2-chlorothiazole-4-carboxylate
CAS:<p>Versatile small molecule scaffold</p>Formula:C6H5BrClNO2SPurity:Min. 95%Molecular weight:270.5 g/mol



