7-Chloro-1H-indazole is a heterocyclic organic compound characterized by its indazole structure, which consists of a five-membered ring fused to a six-membered benzene ring. The presence of a chlorine atom at the 7-position of the indazole ring significantly influences its chemical properties and reactivity. This compound typically exhibits a pale yellow to off-white crystalline appearance and is soluble in organic solvents such as dimethyl sulfoxide (DMSO) and ethanol, but may have limited solubility in water. 7-Chloro-1H-indazole is of interest in medicinal chemistry due to its potential biological activities, including anti-inflammatory and anticancer properties. Its molecular structure allows for various substitutions, which can lead to derivatives with enhanced pharmacological effects. The compound's stability and reactivity can be influenced by the presence of the chlorine atom, which can participate in electrophilic substitution reactions. Overall, 7-chloro-1H-indazole serves as a valuable scaffold in drug discovery and development, warranting further investigation into its therapeutic applications.

7-chloro-1H-indazole

37435-12-4: 7-Chloro-1H-indazole is a heterocyclic organic compound characterized by its indazole structure, which consists of a five-membered ring fused to a six-membered benzene ring. The presence of a chlorine atom at the 7-position of the indazole ring significantly influences its chemical properties and reactivity. This compound typically exhibits a pale yellow to off-white crystalline appearance and is soluble in organic solvents such as dimethyl sulfoxide (DMSO) and ethanol, but may have limited solubility in water. 7-Chloro-1H-indazole is of interest in medicinal chemistry due to its potential biological activities, including anti-inflammatory and anticancer properties. Its molecular structure allows for various substitutions, which can lead to derivatives with enhanced pharmacological effects. The compound's stability and reactivity can be influenced by the presence of the chlorine atom, which can participate in electrophilic substitution reactions. Overall, 7-chloro-1H-indazole serves as a valuable scaffold in drug discovery and development, warranting further investigation into its therapeutic applications.

CAS 37435-12-4

7-chloro-1H-indazole

7-Chloro-1H-indazole

Ref: 54-OR3680

7-Chloro-1H-indazole

Ref: 10-F067652

7-CHLORO-1H-INDAZOLE

Ref: 10-F792197