Ethyl 5-acetyl-2-methylfuran-3-carboxylate, with the CAS number 19615-50-0, is an organic compound characterized by its furan ring structure, which is a five-membered aromatic ring containing oxygen. This compound features an ethyl ester functional group, an acetyl group, and a methyl substituent, contributing to its chemical reactivity and potential applications. It is typically a colorless to pale yellow liquid with a distinctive odor, indicative of its organic nature. The presence of the carboxylate group suggests it may exhibit moderate polarity, influencing its solubility in various organic solvents. Ethyl 5-acetyl-2-methylfuran-3-carboxylate may be utilized in synthetic organic chemistry, particularly in the synthesis of more complex molecules or as an intermediate in the production of pharmaceuticals and agrochemicals. Its reactivity can be attributed to the electrophilic nature of the carbonyl groups, making it a candidate for various chemical reactions, including nucleophilic additions and condensation reactions. Safety data should be consulted for handling and storage, as with all chemical substances.

ethyl 5-acetyl-2-methylfuran-3-carboxylate

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Ethyl 5-acetyl-2-methyl-3-furoate is a semicarbazone that has been shown to have oxidized, furan ring and functional group. The compound is an ester of acetic acid and 2,5-furandione. It is a selenium containing compound. Ethyl 5-acetyl-2-methyl-3-furoate has been found to be effective against methicillin resistant Staphylococcus aureus (MRSA) and Clostridium perfringens, but not against Mycobacterium tuberculosis or Mycobacterium avium complex.

CAS 19615-50-0: ethyl 5-acetyl-2-methylfuran-3-carboxylate

Ethyl 5-acetyl-2-methyl-3-furoate

Ref: 3D-FE131464

Ethyl 5-acetyl-2-methyl-3-furoate

Ref: 10-F314632

ethyl 5-acetyl-2-methyl-3-furoate

Ref: IN-DA00ABAN