3-(Phenylthio)-1H-Indole is an organic compound characterized by its indole structure, which consists of a fused benzene and pyrrole ring. The presence of a phenylthio group at the 3-position of the indole ring introduces unique chemical properties, including potential reactivity and interactions due to the sulfur atom. This compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. Its molecular structure suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, as indole derivatives are known for their biological activity. The phenylthio group can influence the compound's electronic properties and steric hindrance, affecting its interaction with biological targets. Additionally, 3-(Phenylthio)-1H-Indole may participate in various chemical reactions, such as electrophilic substitutions or nucleophilic attacks, making it a versatile building block in organic synthesis. Safety and handling precautions should be observed, as with many sulfur-containing compounds, due to potential toxicity or reactivity.

3-(phenylthio)-1H-Indole

54491-43-9: 3-(Phenylthio)-1H-Indole is an organic compound characterized by its indole structure, which consists of a fused benzene and pyrrole ring. The presence of a phenylthio group at the 3-position of the indole ring introduces unique chemical properties, including potential reactivity and interactions due to the sulfur atom. This compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. Its molecular structure suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, as indole derivatives are known for their biological activity. The phenylthio group can influence the compound's electronic properties and steric hindrance, affecting its interaction with biological targets. Additionally, 3-(Phenylthio)-1H-Indole may participate in various chemical reactions, such as electrophilic substitutions or nucleophilic attacks, making it a versatile building block in organic synthesis. Safety and handling precautions should be observed, as with many sulfur-containing compounds, due to potential toxicity or reactivity.

Tubulin polymerization-IN-74

<p>Tubulin polymerization-IN-74 (compound 11) is an inhibitor of tubulin polymerization, with an IC50 value of 15 μM. It is applicable to cancer research.</p>

CAS 54491-43-9

3-(phenylthio)-1H-Indole

Tubulin polymerization-IN-74

Ref: 54-OR1042114

Tubulin polymerization-IN-74

Ref: TM-T204292