The chemical substance known as (5E)-5-[4-(propan-2-yloxy)benzylidene]-2-sulfanyl-1,3-thiazol-4(5H)-one, with the CAS number 303798-03-0, is characterized by its thiazole core, which is a five-membered heterocyclic ring containing sulfur and nitrogen. This compound features a benzylidene moiety, indicating the presence of an aldehyde functional group attached to a benzene ring, which is further substituted with a propan-2-yloxy group, enhancing its lipophilicity and potentially influencing its biological activity. The thiazolone structure contributes to its reactivity, particularly in nucleophilic addition reactions. The presence of the sulfanyl group suggests potential for thiol-related chemistry, which can be significant in various biochemical interactions. This compound may exhibit interesting pharmacological properties, making it a subject of interest in medicinal chemistry. Its unique structural features could lead to diverse applications, including in drug development or as a biochemical probe, although specific biological activities would require empirical investigation.

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

303798-03-0: The chemical substance known as (5E)-5-[4-(propan-2-yloxy)benzylidene]-2-sulfanyl-1,3-thiazol-4(5H)-one, with the CAS number 303798-03-0, is characterized by its thiazole core, which is a five-membered heterocyclic ring containing sulfur and nitrogen. This compound features a benzylidene moiety, indicating the presence of an aldehyde functional group attached to a benzene ring, which is further substituted with a propan-2-yloxy group, enhancing its lipophilicity and potentially influencing its biological activity. The thiazolone structure contributes to its reactivity, particularly in nucleophilic addition reactions. The presence of the sulfanyl group suggests potential for thiol-related chemistry, which can be significant in various biochemical interactions. This compound may exhibit interesting pharmacological properties, making it a subject of interest in medicinal chemistry. Its unique structural features could lead to diverse applications, including in drug development or as a biochemical probe, although specific biological activities would require empirical investigation.

CAS 303798-03-0

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

(5E)-5-(4-Isopropoxybenzylidene)-2-mercapto-1,3-thiazol-4(5H)-one

Ref: IN-DA002ZWY

(5E)-5-(4-isopropoxybenzylidene)-2-mercapto-1,3-thiazol-4(5H)-one

Ref: 10-F307832