4,5-Dihydro-3-benzothiepin-1(2H)-one, with the CAS number 51659-38-2, is a heterocyclic organic compound characterized by its unique bicyclic structure that incorporates a benzothiepin moiety. This compound features a sulfur atom within its ring system, contributing to its chemical properties and reactivity. Typically, benzothiepin derivatives exhibit interesting biological activities, making them of interest in medicinal chemistry. The presence of the dihydro group indicates that the compound has a saturated bond in the bicyclic structure, which can influence its stability and interaction with biological targets. In terms of physical properties, compounds of this class may exhibit moderate solubility in organic solvents and possess specific melting and boiling points that are characteristic of similar heterocycles. The compound's potential applications may include roles in pharmaceuticals, particularly in the development of drugs targeting various diseases, owing to the biological significance of sulfur-containing heterocycles. However, specific data regarding its toxicity, environmental impact, and detailed reactivity would require further investigation and analysis.

4,5-dihydro-3-benzothiepin-1(2H)-one

51659-38-2: 4,5-Dihydro-3-benzothiepin-1(2H)-one, with the CAS number 51659-38-2, is a heterocyclic organic compound characterized by its unique bicyclic structure that incorporates a benzothiepin moiety. This compound features a sulfur atom within its ring system, contributing to its chemical properties and reactivity. Typically, benzothiepin derivatives exhibit interesting biological activities, making them of interest in medicinal chemistry. The presence of the dihydro group indicates that the compound has a saturated bond in the bicyclic structure, which can influence its stability and interaction with biological targets. In terms of physical properties, compounds of this class may exhibit moderate solubility in organic solvents and possess specific melting and boiling points that are characteristic of similar heterocycles. The compound's potential applications may include roles in pharmaceuticals, particularly in the development of drugs targeting various diseases, owing to the biological significance of sulfur-containing heterocycles. However, specific data regarding its toxicity, environmental impact, and detailed reactivity would require further investigation and analysis.

CAS 51659-38-2

4,5-dihydro-3-benzothiepin-1(2H)-one

1,2,4,5-Tetrahydro-3-benzothiepin-1-one

Ref: 3D-BCA65938