The chemical substance known as (5E)-5-[2-(2-methylpropoxy)benzylidene]-2-sulfanyl-1,3-thiazol-4(5H)-one, with the CAS number 669747-27-7, is characterized by its thiazole core, which is a five-membered heterocyclic compound containing sulfur and nitrogen. This compound features a benzylidene group, indicating the presence of an aldehyde functional group attached to a benzene ring, which contributes to its reactivity and potential biological activity. The presence of a sulfanyl group (–SH) enhances its potential for forming disulfide bonds, which can be significant in biochemical interactions. The 2-methylpropoxy substituent adds hydrophobic characteristics, influencing its solubility and interaction with biological membranes. Overall, this compound may exhibit interesting pharmacological properties, making it a subject of interest in medicinal chemistry and drug development. Its structural complexity suggests potential applications in various fields, including pharmaceuticals, where thiazole derivatives are often explored for their antimicrobial, anti-inflammatory, and anticancer activities.

(5E)-5-[2-(2-methylpropoxy)benzylidene]-2-sulfanyl-1,3-thiazol-4(5H)-one

669747-27-7: The chemical substance known as (5E)-5-[2-(2-methylpropoxy)benzylidene]-2-sulfanyl-1,3-thiazol-4(5H)-one, with the CAS number 669747-27-7, is characterized by its thiazole core, which is a five-membered heterocyclic compound containing sulfur and nitrogen. This compound features a benzylidene group, indicating the presence of an aldehyde functional group attached to a benzene ring, which contributes to its reactivity and potential biological activity. The presence of a sulfanyl group (–SH) enhances its potential for forming disulfide bonds, which can be significant in biochemical interactions. The 2-methylpropoxy substituent adds hydrophobic characteristics, influencing its solubility and interaction with biological membranes. Overall, this compound may exhibit interesting pharmacological properties, making it a subject of interest in medicinal chemistry and drug development. Its structural complexity suggests potential applications in various fields, including pharmaceuticals, where thiazole derivatives are often explored for their antimicrobial, anti-inflammatory, and anticancer activities.

CAS 669747-27-7

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