3-(4-Bromophenyl)-2H-1,2,4-oxadiazol-5-one is a heterocyclic compound characterized by the presence of an oxadiazole ring, which is a five-membered ring containing two nitrogen atoms and three carbon atoms. The compound features a bromophenyl substituent, which enhances its chemical reactivity and potential applications in various fields, including pharmaceuticals and agrochemicals. Its structure contributes to its unique properties, such as stability under certain conditions and the ability to participate in various chemical reactions, including nucleophilic substitutions and cycloadditions. The presence of the bromine atom can also influence its electronic properties, making it a useful building block in organic synthesis. Additionally, compounds of this class may exhibit biological activity, making them of interest in medicinal chemistry. The CAS number 16672-19-8 provides a unique identifier for this substance, facilitating its identification in chemical databases and literature. Overall, this compound exemplifies the diverse chemistry associated with oxadiazole derivatives.

3-(4-bromophenyl)-2H-1,2,4-oxadiazol-5-one

16672-19-8: 3-(4-Bromophenyl)-2H-1,2,4-oxadiazol-5-one is a heterocyclic compound characterized by the presence of an oxadiazole ring, which is a five-membered ring containing two nitrogen atoms and three carbon atoms. The compound features a bromophenyl substituent, which enhances its chemical reactivity and potential applications in various fields, including pharmaceuticals and agrochemicals. Its structure contributes to its unique properties, such as stability under certain conditions and the ability to participate in various chemical reactions, including nucleophilic substitutions and cycloadditions. The presence of the bromine atom can also influence its electronic properties, making it a useful building block in organic synthesis. Additionally, compounds of this class may exhibit biological activity, making them of interest in medicinal chemistry. The CAS number 16672-19-8 provides a unique identifier for this substance, facilitating its identification in chemical databases and literature. Overall, this compound exemplifies the diverse chemistry associated with oxadiazole derivatives.

3-(4-Bromophenyl)-1,2,4-oxadiazol-5(4H)-one

CAS 16672-19-8

3-(4-bromophenyl)-2H-1,2,4-oxadiazol-5-one

3-(4-Bromophenyl)-1,2,4-oxadiazol-5(4H)-one

Ref: 54-OR909899

3-(4-Bromophenyl)-1,2,4-Oxadiazol-5(4H)-One

Ref: IN-DA001WWA

3-(4-Bromophenyl)-1,2,4-oxadiazol-5(4H)-one

Ref: IN-DG243414