1H-Indazole-5-thiol is a heterocyclic organic compound characterized by its indazole core, which consists of a fused five-membered ring containing two nitrogen atoms. The presence of a thiol (-SH) group at the 5-position of the indazole ring is a notable feature, imparting unique chemical reactivity and properties. This compound is typically a solid at room temperature and may exhibit moderate solubility in polar solvents due to the thiol group. 1H-Indazole-5-thiol can participate in various chemical reactions, including nucleophilic substitutions and oxidation, making it valuable in synthetic organic chemistry and medicinal chemistry. Its potential applications include serving as a building block for pharmaceuticals and agrochemicals, as well as in the development of materials with specific electronic or optical properties. Additionally, the compound may exhibit biological activity, which warrants further investigation for its potential therapeutic uses. As with many thiol-containing compounds, it is important to handle 1H-Indazole-5-thiol with care due to its potential reactivity and the odor associated with thiols.

1H-Indazole-5-thiol

569339-86-2: 1H-Indazole-5-thiol is a heterocyclic organic compound characterized by its indazole core, which consists of a fused five-membered ring containing two nitrogen atoms. The presence of a thiol (-SH) group at the 5-position of the indazole ring is a notable feature, imparting unique chemical reactivity and properties. This compound is typically a solid at room temperature and may exhibit moderate solubility in polar solvents due to the thiol group. 1H-Indazole-5-thiol can participate in various chemical reactions, including nucleophilic substitutions and oxidation, making it valuable in synthetic organic chemistry and medicinal chemistry. Its potential applications include serving as a building block for pharmaceuticals and agrochemicals, as well as in the development of materials with specific electronic or optical properties. Additionally, the compound may exhibit biological activity, which warrants further investigation for its potential therapeutic uses. As with many thiol-containing compounds, it is important to handle 1H-Indazole-5-thiol with care due to its potential reactivity and the odor associated with thiols.

CAS 569339-86-2

1H-Indazole-5-thiol

1H-Indazole-5-thiol

Ref: IN-DA00F2L3

5-Sulphanyl-1H-indazole

Ref: 54-OR305638

1H-Indazole-5-thiol

Ref: 3D-UXA33986