4-(2-Furyl)-2-pyrimidinethiol is an organic compound characterized by its unique structure, which includes a pyrimidine ring and a furyl group. This compound typically exhibits properties associated with both heterocyclic compounds and thiols, such as potential reactivity due to the presence of the thiol (-SH) functional group. It may display moderate solubility in polar solvents, while its aromatic components contribute to its stability and potential for π-π stacking interactions. The presence of the furyl group can impart specific electronic properties, making it of interest in various chemical applications, including medicinal chemistry and material science. Additionally, compounds like this can participate in redox reactions due to the thiol group, which can be oxidized to form disulfides or sulfenic acids. Its biological activity may also be explored, as thiol-containing compounds often play roles in biological systems, including enzyme function and antioxidant activity. Overall, 4-(2-furyl)-2-pyrimidinethiol represents a versatile structure with potential applications in various fields of chemistry.

4-(2-FURYL)-2-PYRIMIDINETHIOL

190579-95-4: 4-(2-Furyl)-2-pyrimidinethiol is an organic compound characterized by its unique structure, which includes a pyrimidine ring and a furyl group. This compound typically exhibits properties associated with both heterocyclic compounds and thiols, such as potential reactivity due to the presence of the thiol (-SH) functional group. It may display moderate solubility in polar solvents, while its aromatic components contribute to its stability and potential for π-π stacking interactions. The presence of the furyl group can impart specific electronic properties, making it of interest in various chemical applications, including medicinal chemistry and material science. Additionally, compounds like this can participate in redox reactions due to the thiol group, which can be oxidized to form disulfides or sulfenic acids. Its biological activity may also be explored, as thiol-containing compounds often play roles in biological systems, including enzyme function and antioxidant activity. Overall, 4-(2-furyl)-2-pyrimidinethiol represents a versatile structure with potential applications in various fields of chemistry.

CAS 190579-95-4

4-(2-FURYL)-2-PYRIMIDINETHIOL

2(1H)-Pyrimidinethione, 6-(2-furanyl)-

Ref: IN-DA002EMW

4-(2-Furyl)pyrimidine-2-thiol

Ref: 54-OR97895

4-Furan-2-yl-pyrimidine-2-thiol

Ref: 10-F025950