1H-Indazole, 7-methyl- is an organic compound characterized by its indazole core, which consists of a five-membered ring fused to a six-membered aromatic ring. The presence of a methyl group at the 7-position of the indazole structure contributes to its unique chemical properties. This compound is typically a colorless to pale yellow solid and is soluble in organic solvents. It exhibits moderate stability under standard conditions but may be sensitive to strong oxidizing agents. 1H-Indazole derivatives are of interest in medicinal chemistry due to their potential biological activities, including anti-inflammatory and anticancer properties. The compound's molecular structure allows for various substitution patterns, which can influence its reactivity and interactions with biological targets. As with many indazole derivatives, it may participate in various chemical reactions, including electrophilic aromatic substitution and nucleophilic addition, making it a versatile building block in organic synthesis. Safety data should be consulted for handling and storage, as with all chemical substances.

1H-Indazole, 7-methyl-

3176-66-7: 1H-Indazole, 7-methyl- is an organic compound characterized by its indazole core, which consists of a five-membered ring fused to a six-membered aromatic ring. The presence of a methyl group at the 7-position of the indazole structure contributes to its unique chemical properties. This compound is typically a colorless to pale yellow solid and is soluble in organic solvents. It exhibits moderate stability under standard conditions but may be sensitive to strong oxidizing agents. 1H-Indazole derivatives are of interest in medicinal chemistry due to their potential biological activities, including anti-inflammatory and anticancer properties. The compound's molecular structure allows for various substitution patterns, which can influence its reactivity and interactions with biological targets. As with many indazole derivatives, it may participate in various chemical reactions, including electrophilic aromatic substitution and nucleophilic addition, making it a versatile building block in organic synthesis. Safety data should be consulted for handling and storage, as with all chemical substances.

CAS 3176-66-7

1H-Indazole, 7-methyl-

7-Methyl-1H-indazole

Ref: IN-DA00382R

7-Methyl-1H-indazole

Ref: 54-OR928851

7-Methyl-1H-indazole

Ref: 10-F076205