Ethyl 2-[(chloroacetyl)amino]-4-methyl-5-phenylthiophene-3-carboxylate, with the CAS number 731820-85-2, is a synthetic organic compound characterized by its complex structure, which includes a thiophene ring, an ethyl ester group, and a chloroacetylamino substituent. This compound typically exhibits properties associated with both aromatic and heterocyclic compounds, such as potential biological activity and solubility in organic solvents. The presence of the chloroacetyl group may impart reactivity, making it useful in various chemical reactions, including nucleophilic substitutions. Its thiophene moiety contributes to its electronic properties, potentially allowing for interactions with biological targets. Ethyl esters generally have moderate volatility and can be hydrolyzed to their corresponding acids. The compound's specific applications may include roles in pharmaceuticals or agrochemicals, where its unique structure could confer desirable biological activities. As with many synthetic compounds, safety data should be consulted to understand its handling and toxicity profiles.

ETHYL 2-[(CHLOROACETYL)AMINO]-4-METHYL-5-PHENYLTHIOPHENE-3-CARBOXYLATE

731820-85-2: Ethyl 2-[(chloroacetyl)amino]-4-methyl-5-phenylthiophene-3-carboxylate, with the CAS number 731820-85-2, is a synthetic organic compound characterized by its complex structure, which includes a thiophene ring, an ethyl ester group, and a chloroacetylamino substituent. This compound typically exhibits properties associated with both aromatic and heterocyclic compounds, such as potential biological activity and solubility in organic solvents. The presence of the chloroacetyl group may impart reactivity, making it useful in various chemical reactions, including nucleophilic substitutions. Its thiophene moiety contributes to its electronic properties, potentially allowing for interactions with biological targets. Ethyl esters generally have moderate volatility and can be hydrolyzed to their corresponding acids. The compound's specific applications may include roles in pharmaceuticals or agrochemicals, where its unique structure could confer desirable biological activities. As with many synthetic compounds, safety data should be consulted to understand its handling and toxicity profiles.

<p>Ethyl 2-(2-chloroacetamido)-4-methyl-5-phenylthiophene-3-carboxylate</p>

CAS 731820-85-2

ETHYL 2-[(CHLOROACETYL)AMINO]-4-METHYL-5-PHENYLTHIOPHENE-3-CARBOXYLATE

Ethyl 2-(2-chloroacetamido)-4-methyl-5-phenylthiophene-3-carboxylate

Ref: 54-OR85096

Ethyl 2-(2-chloroacetamido)-4-methyl-5-phenylthiophene-3-carboxylate

Ref: 10-F643362