4-Methoxy-1H-indazole is a chemical compound characterized by its indazole core, which is a bicyclic structure containing a five-membered ring fused to a six-membered ring. The presence of a methoxy group (-OCH3) at the 4-position of the indazole ring significantly influences its chemical properties and reactivity. This compound is typically a white to off-white solid and is soluble in organic solvents. It exhibits potential biological activity, making it of interest in medicinal chemistry and pharmacology. The methoxy group can enhance lipophilicity, potentially affecting the compound's ability to cross biological membranes. Additionally, 4-methoxy-1H-indazole may participate in various chemical reactions, including electrophilic substitutions and nucleophilic attacks, due to the electron-donating nature of the methoxy group. Its unique structure and properties make it a subject of research in various fields, including drug development and material science. As with any chemical substance, proper handling and safety precautions should be observed when working with 4-methoxy-1H-indazole.

4-methoxy-1H-indazole

4-Methoxy-1H-indazole

4-Methoxy-1H-indazole is a synthetic chemical that can be synthesized from ketones and methanol. This chemical has been made in high yield by reacting methoxyacetone with toluene in tetrahydrofuran, followed by an anhydride reaction with ethyl ketone. The synthesis of this compound involves the use of a variety of organic solvents and reagents, as well as the use of a variety of different techniques.

CAS 351210-06-5: 4-methoxy-1H-indazole

4-Methoxy-1H-indazole

Ref: IN-DA003436

4-Methoxy-1H-indazole

Ref: 3D-FM160679

4-Methoxy-1H-indazole

Ref: 10-F093611

4-Methoxy-1H-indazole

Ref: 54-OR305095