5-Methyl-1H-indazole is an organic compound characterized by its indazole structure, which consists of a five-membered ring fused to a six-membered aromatic ring. This compound features a methyl group attached to the nitrogen-containing ring, specifically at the 5-position. It is typically a colorless to pale yellow solid with moderate solubility in organic solvents. The molecular formula of 5-Methyl-1H-indazole reflects its composition of carbon, hydrogen, and nitrogen atoms, contributing to its aromatic properties. This compound is of interest in various fields, including medicinal chemistry and material science, due to its potential biological activities and applications in drug development. Its reactivity can be influenced by the presence of the methyl group, which may affect its electronic properties and interactions with other molecules. Additionally, 5-Methyl-1H-indazole can undergo various chemical reactions, such as substitution and oxidation, making it a versatile building block in synthetic organic chemistry. Safety data should be consulted for handling and storage, as with any chemical substance.

5-Methyl-1H-Indazole

1776-37-0: 5-Methyl-1H-indazole is an organic compound characterized by its indazole structure, which consists of a five-membered ring fused to a six-membered aromatic ring. This compound features a methyl group attached to the nitrogen-containing ring, specifically at the 5-position. It is typically a colorless to pale yellow solid with moderate solubility in organic solvents. The molecular formula of 5-Methyl-1H-indazole reflects its composition of carbon, hydrogen, and nitrogen atoms, contributing to its aromatic properties. This compound is of interest in various fields, including medicinal chemistry and material science, due to its potential biological activities and applications in drug development. Its reactivity can be influenced by the presence of the methyl group, which may affect its electronic properties and interactions with other molecules. Additionally, 5-Methyl-1H-indazole can undergo various chemical reactions, such as substitution and oxidation, making it a versatile building block in synthetic organic chemistry. Safety data should be consulted for handling and storage, as with any chemical substance.

CAS 1776-37-0

5-Methyl-1H-Indazole

1H-Indazole, 5-methyl-

Ref: IN-DA0025F0

5-Methyl-1H-indazole

Ref: 54-OR305086

5-Methyl-1H-indazole

Ref: 10-F079331