Ethyl 2-(5-bromo-2-thienyl)-2-oxoacetate is an organic compound characterized by its thienyl and bromo substituents, which contribute to its unique chemical properties. The presence of the thienyl group, a five-membered aromatic ring containing sulfur, imparts notable electronic characteristics, enhancing the compound's reactivity and potential applications in organic synthesis. The bromo substituent serves as a versatile functional group, allowing for further chemical modifications through nucleophilic substitution reactions. The ester functional group in the molecule indicates that it can undergo hydrolysis, transesterification, or other reactions typical of esters. Ethyl 2-(5-bromo-2-thienyl)-2-oxoacetate is likely to exhibit moderate solubility in organic solvents, and its reactivity may be influenced by the electron-withdrawing effects of the bromo and carbonyl groups. This compound may find applications in pharmaceuticals, agrochemicals, or as an intermediate in the synthesis of more complex organic molecules. As with many chemical substances, proper handling and safety precautions are essential due to potential toxicity or reactivity.

ethyl 2-(5-bromo-2-thienyl)-2-oxoacetate

22098-10-8: Ethyl 2-(5-bromo-2-thienyl)-2-oxoacetate is an organic compound characterized by its thienyl and bromo substituents, which contribute to its unique chemical properties. The presence of the thienyl group, a five-membered aromatic ring containing sulfur, imparts notable electronic characteristics, enhancing the compound's reactivity and potential applications in organic synthesis. The bromo substituent serves as a versatile functional group, allowing for further chemical modifications through nucleophilic substitution reactions. The ester functional group in the molecule indicates that it can undergo hydrolysis, transesterification, or other reactions typical of esters. Ethyl 2-(5-bromo-2-thienyl)-2-oxoacetate is likely to exhibit moderate solubility in organic solvents, and its reactivity may be influenced by the electron-withdrawing effects of the bromo and carbonyl groups. This compound may find applications in pharmaceuticals, agrochemicals, or as an intermediate in the synthesis of more complex organic molecules. As with many chemical substances, proper handling and safety precautions are essential due to potential toxicity or reactivity.

CAS 22098-10-8

ethyl 2-(5-bromo-2-thienyl)-2-oxoacetate

Ethyl 2-(5-bromothiophen-2-yl)-2-oxoacetate

Ref: IN-DA00709K

Ethyl (5-bromothien-2-yl)(oxo)acetate

Ref: 54-OR6743