1H-Indazole,6-(2-thienyl)- is a heterocyclic organic compound characterized by its indazole core, which consists of a five-membered ring containing two nitrogen atoms, fused to a six-membered thienyl ring. This compound exhibits properties typical of both indazoles and thiophene derivatives, including potential aromaticity and electron-rich characteristics due to the presence of nitrogen and sulfur atoms. The thienyl group contributes to its unique electronic properties, potentially enhancing its reactivity and interactions in various chemical environments. 1H-Indazole,6-(2-thienyl)- may exhibit biological activity, making it of interest in medicinal chemistry and drug development. Its structural features suggest it could participate in various chemical reactions, including electrophilic substitutions and coordination with metal ions. The compound's solubility, stability, and reactivity can be influenced by the substituents on the indazole and thienyl rings, which can be tailored for specific applications in research and industry. Overall, this compound represents a versatile scaffold for further exploration in synthetic and medicinal chemistry.

1H-Indazole,6-(2-thienyl)-

885272-10-6: 1H-Indazole,6-(2-thienyl)- is a heterocyclic organic compound characterized by its indazole core, which consists of a five-membered ring containing two nitrogen atoms, fused to a six-membered thienyl ring. This compound exhibits properties typical of both indazoles and thiophene derivatives, including potential aromaticity and electron-rich characteristics due to the presence of nitrogen and sulfur atoms. The thienyl group contributes to its unique electronic properties, potentially enhancing its reactivity and interactions in various chemical environments. 1H-Indazole,6-(2-thienyl)- may exhibit biological activity, making it of interest in medicinal chemistry and drug development. Its structural features suggest it could participate in various chemical reactions, including electrophilic substitutions and coordination with metal ions. The compound's solubility, stability, and reactivity can be influenced by the substituents on the indazole and thienyl rings, which can be tailored for specific applications in research and industry. Overall, this compound represents a versatile scaffold for further exploration in synthetic and medicinal chemistry.

CAS 885272-10-6

1H-Indazole,6-(2-thienyl)-

6-(Thiophen-2-yl)-1H-indazole

Ref: IN-DA0046XP

6-(Thiophen-2-yl)-1H-indazole

Ref: 10-F457431