1-(2-(2-Chlorophenoxy)acetyl)-4-(4-methoxyphenyl)thiosemicarbazide is a chemical compound characterized by its thiosemicarbazide structure, which features a thiosemicarbazide moiety linked to an aromatic system. This compound typically exhibits properties associated with thiosemicarbazides, such as potential biological activity, including antimicrobial and anticancer effects. The presence of the chlorophenoxy and methoxyphenyl groups suggests that it may have enhanced lipophilicity and the ability to interact with biological targets. The chlorophenoxy group can contribute to the compound's reactivity and solubility in organic solvents, while the methoxy group may influence its electronic properties and steric hindrance. Additionally, the thiosemicarbazide functional group is known for its ability to form coordination complexes with metal ions, which can be relevant in medicinal chemistry. Overall, this compound's unique structure may lead to diverse applications in pharmaceuticals and agrochemicals, although specific biological activities and mechanisms would require further investigation.

1-(2-(2-CHLOROPHENOXY)ACETYL)-4-(4-METHOXYPHENYL)THIOSEMICARBAZIDE

91543-59-8: 1-(2-(2-Chlorophenoxy)acetyl)-4-(4-methoxyphenyl)thiosemicarbazide is a chemical compound characterized by its thiosemicarbazide structure, which features a thiosemicarbazide moiety linked to an aromatic system. This compound typically exhibits properties associated with thiosemicarbazides, such as potential biological activity, including antimicrobial and anticancer effects. The presence of the chlorophenoxy and methoxyphenyl groups suggests that it may have enhanced lipophilicity and the ability to interact with biological targets. The chlorophenoxy group can contribute to the compound's reactivity and solubility in organic solvents, while the methoxy group may influence its electronic properties and steric hindrance. Additionally, the thiosemicarbazide functional group is known for its ability to form coordination complexes with metal ions, which can be relevant in medicinal chemistry. Overall, this compound's unique structure may lead to diverse applications in pharmaceuticals and agrochemicals, although specific biological activities and mechanisms would require further investigation.

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CAS 91543-59-8

1-(2-(2-CHLOROPHENOXY)ACETYL)-4-(4-METHOXYPHENYL)THIOSEMICARBAZIDE

1-(2-(2-chlorophenoxy)acetyl)-4-(4-methoxyphenyl)thiosemicarbazide

Ref: 3D-RDA54359