3-Methyl-1H-indazole is an 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 methyl group at the third position of the indazole ring influences its chemical properties and reactivity. This compound is typically a white to off-white solid and is soluble in organic solvents such as ethanol and dimethyl sulfoxide (DMSO), but may have limited solubility in water. 3-Methyl-1H-indazole is of interest in various fields, including medicinal chemistry, due to its potential biological activities and applications in drug development. It may exhibit properties such as anti-inflammatory, analgesic, or anticancer effects, although specific biological activities can vary based on structural modifications and the presence of substituents. As with many indazole derivatives, it is important to handle this compound with care, following appropriate safety protocols, as it may pose health risks or environmental hazards.

3-Methyl-1H-indazole is a heterocyclic alkyl compound containing nitrogen and three methyl groups. It is used as an intermediate in the synthesis of other compounds. It has been shown to have anti-inflammatory properties in vitro. It also inhibits neutrophil chemotaxis and may be used to treat inflammatory diseases such as trigeminal neuralgia or heart disease. 3-Methyl-1H-indazole has also been shown to inhibit histamine H3 receptor activity, which may account for its effects on eye diseases and bladder cancer.

3-Methyl-1H-indazole

3176-62-3: 3-Methyl-1H-indazole is an 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 methyl group at the third position of the indazole ring influences its chemical properties and reactivity. This compound is typically a white to off-white solid and is soluble in organic solvents such as ethanol and dimethyl sulfoxide (DMSO), but may have limited solubility in water. 3-Methyl-1H-indazole is of interest in various fields, including medicinal chemistry, due to its potential biological activities and applications in drug development. It may exhibit properties such as anti-inflammatory, analgesic, or anticancer effects, although specific biological activities can vary based on structural modifications and the presence of substituents. As with many indazole derivatives, it is important to handle this compound with care, following appropriate safety protocols, as it may pose health risks or environmental hazards.

CAS 3176-62-3

3-Methyl-1H-indazole

1H-Indazole, 3-methyl-

Ref: IN-DA00I60O

3-Methyl-1H-indazole

Ref: 54-OR912540

3-Methyl-1H-indazole

Ref: 10-F070467