5-(Tetrahydrofuran-2-yl)-1,3,4-oxadiazol-2-amine is a chemical compound characterized by its unique structure, which includes a five-membered oxadiazole ring and a tetrahydrofuran moiety. The presence of the oxadiazole ring imparts specific properties, such as potential biological activity and the ability to participate in various chemical reactions. This compound is likely to exhibit moderate polarity due to the presence of both nitrogen and oxygen atoms in its structure, which can influence its solubility in different solvents. Additionally, the tetrahydrofuran group contributes to its stability and may affect its interaction with biological targets. The amine functional group can engage in hydrogen bonding, enhancing its reactivity and potential applications in medicinal chemistry. Overall, this compound may be of interest in the development of pharmaceuticals or agrochemicals, given the significance of oxadiazole derivatives in these fields. However, specific applications and biological activities would require further investigation through experimental studies.

5-(tetrahydrofuran-2-yl)-1,3,4-oxadiazol-2-amine

502133-68-8: 5-(Tetrahydrofuran-2-yl)-1,3,4-oxadiazol-2-amine is a chemical compound characterized by its unique structure, which includes a five-membered oxadiazole ring and a tetrahydrofuran moiety. The presence of the oxadiazole ring imparts specific properties, such as potential biological activity and the ability to participate in various chemical reactions. This compound is likely to exhibit moderate polarity due to the presence of both nitrogen and oxygen atoms in its structure, which can influence its solubility in different solvents. Additionally, the tetrahydrofuran group contributes to its stability and may affect its interaction with biological targets. The amine functional group can engage in hydrogen bonding, enhancing its reactivity and potential applications in medicinal chemistry. Overall, this compound may be of interest in the development of pharmaceuticals or agrochemicals, given the significance of oxadiazole derivatives in these fields. However, specific applications and biological activities would require further investigation through experimental studies.

CAS 502133-68-8

5-(tetrahydrofuran-2-yl)-1,3,4-oxadiazol-2-amine

5-(Tetrahydrofuran-2-yl)-1,3,4-oxadiazol-2-amine

Ref: IN-DA006VQH

5-(tetrahydro-2-furanyl)-1,3,4-oxadiazol-2-amine

Ref: 10-F311841

5-(Tetrahydrofuran-2-yl)-1,3,4-oxadiazol-2-amine

Ref: 3D-CVA13368