1H-Indazole,6-(3-thienyl)- is an organic compound characterized by its indazole core, which is a five-membered ring containing two nitrogen atoms, fused to a thiophene ring (3-thienyl). This compound typically exhibits properties associated with heterocyclic compounds, including potential biological activity due to the presence of nitrogen and sulfur atoms in its structure. The indazole moiety is known for its involvement in various pharmacological activities, making derivatives of this compound of interest in medicinal chemistry. The presence of the thienyl group can influence the compound's electronic properties and solubility, potentially enhancing its reactivity and interaction with biological targets. Additionally, 1H-Indazole,6-(3-thienyl)- may exhibit characteristics such as moderate to high stability under standard conditions, and it may be soluble in organic solvents. Its unique structure allows for various synthetic modifications, which can lead to the development of new derivatives with tailored properties for specific applications in drug discovery and materials science.

1H-Indazole,6-(3-thienyl)-

281203-98-3: 1H-Indazole,6-(3-thienyl)- is an organic compound characterized by its indazole core, which is a five-membered ring containing two nitrogen atoms, fused to a thiophene ring (3-thienyl). This compound typically exhibits properties associated with heterocyclic compounds, including potential biological activity due to the presence of nitrogen and sulfur atoms in its structure. The indazole moiety is known for its involvement in various pharmacological activities, making derivatives of this compound of interest in medicinal chemistry. The presence of the thienyl group can influence the compound's electronic properties and solubility, potentially enhancing its reactivity and interaction with biological targets. Additionally, 1H-Indazole,6-(3-thienyl)- may exhibit characteristics such as moderate to high stability under standard conditions, and it may be soluble in organic solvents. Its unique structure allows for various synthetic modifications, which can lead to the development of new derivatives with tailored properties for specific applications in drug discovery and materials science.

CAS 281203-98-3

1H-Indazole,6-(3-thienyl)-

6-(Thiophen-3-yl)-1H-indazole

Ref: IN-DA00C3DY

6-(Thiophen-3-yl)-1H-indazole

Ref: 10-F456753