Ethyl (6R)-2-[(chloroacetyl)amino]-6-methyl-4,5,6,7-tetrahydro-1-benzothiophene-3-carboxylate, with CAS number 76981-87-8, is a chemical compound characterized by its complex structure, which includes a benzothiophene core. This compound features a chloroacetyl group and an ethyl ester functional group, contributing to its reactivity and potential biological activity. The presence of the tetrahydro structure indicates that it is a saturated derivative, which may influence its solubility and stability. The specific stereochemistry at the 6R position suggests that it may exhibit chirality, potentially leading to different biological effects depending on the enantiomer. This compound may be of interest in medicinal chemistry due to its structural features, which could be linked to various pharmacological activities. Its synthesis and characterization would typically involve standard organic chemistry techniques, and it may be studied for its potential applications in drug development or as a biochemical probe. Safety and handling precautions should be observed due to the presence of the chloroacetyl moiety, which can be reactive.

ethyl (6R)-2-[(chloroacetyl)amino]-6-methyl-4,5,6,7-tetrahydro-1-benzothiophene-3-carboxylate

76981-87-8: Ethyl (6R)-2-[(chloroacetyl)amino]-6-methyl-4,5,6,7-tetrahydro-1-benzothiophene-3-carboxylate, with CAS number 76981-87-8, is a chemical compound characterized by its complex structure, which includes a benzothiophene core. This compound features a chloroacetyl group and an ethyl ester functional group, contributing to its reactivity and potential biological activity. The presence of the tetrahydro structure indicates that it is a saturated derivative, which may influence its solubility and stability. The specific stereochemistry at the 6R position suggests that it may exhibit chirality, potentially leading to different biological effects depending on the enantiomer. This compound may be of interest in medicinal chemistry due to its structural features, which could be linked to various pharmacological activities. Its synthesis and characterization would typically involve standard organic chemistry techniques, and it may be studied for its potential applications in drug development or as a biochemical probe. Safety and handling precautions should be observed due to the presence of the chloroacetyl moiety, which can be reactive.

CAS 76981-87-8

ethyl (6R)-2-[(chloroacetyl)amino]-6-methyl-4,5,6,7-tetrahydro-1-benzothiophene-3-carboxylate

2-(2-Chloro-acetylamino)-6-methyl-4,5,6,7-tetrahydro-benzo[b]thiophene-3-carboxylic acid ethyl ester

Ref: 10-F057839