3-Chloro-N-(2-thienylmethyl)propanamide is an organic compound characterized by its amide functional group, which is derived from propanoic acid. The presence of a chlorine atom at the third carbon position and a thienylmethyl group, which is a thiophene derivative, contributes to its unique chemical properties. This compound typically exhibits moderate polarity due to the amide bond, which can engage in hydrogen bonding, influencing its solubility in polar solvents. The thienylmethyl group may impart additional reactivity and biological activity, making it of interest in medicinal chemistry and drug development. The compound's structure suggests potential applications in various fields, including agrochemicals and pharmaceuticals, where the thienyl moiety can enhance biological activity. Its CAS number, 21403-26-9, allows for easy identification and reference in chemical databases. Safety and handling precautions should be observed, as with many chlorinated compounds, due to potential toxicity and environmental impact.

3-Chloro-N-(2-thienylmethyl)propanamide

21403-26-9: 3-Chloro-N-(2-thienylmethyl)propanamide, 3-Chloro-N-thiophen-2-ylmethyl-propionamide, Propionamide, 3-chloro-N-2-thenyl-, propanamide, 3-chloro-N-(2-thienylmethyl)-, 3-Chloro-N-(thiophen-2-ylmethyl)propanamide

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CAS 21403-26-9: 3-Chloro-N-(2-thienylmethyl)propanamide

3-Chloro-N-(thien-2-ylmethyl)propanamide

Ref: 3D-FC115115

3-chloro-N-(2-thienylmethyl)propanamide

Ref: 10-F315387