Home Chemistry Heterocyclic Building Blocks Indazoles 6-Methoxy-1H-Indazole
Nucleophilic Substitution: The methoxy group (-OCH3) can be displaced by a nucleophile, such as a halide or a thiol, leading to the formation of substituted derivatives.
Electrophilic Substitution: The aromatic ring can undergo electrophilic substitution reactions, such as halogenation, nitration, sulfonation, or Friedel-Crafts acylation/alkylation.
Reduction: The nitro group (-NO2) can be reduced to the corresponding amino group (-NH2) using reducing agents such as hydrogen gas over a metal catalyst or iron filings with acid.
Oxidation: The amino group (-NH2) can be oxidized to various products, including nitro compounds or oximes, under appropriate conditions.
Dehydration: Under acidic conditions, dehydration reactions can occur to eliminate water and form unsaturated compounds.
Ring-cleavage Reactions: The ring structure can undergo cleavage under certain conditions, leading to the formation of smaller molecules.
Condensation Reactions: It can participate in condensation reactions with carbonyl compounds or other nucleophiles to form cyclic compounds or larger molecules.
Metalation: The indazole ring can be metalated at the 5-position under certain conditions, allowing for further reactions with electrophiles or nucleophiles.
Framework+−
By Key Group+−
By Parent Nucleus+−
By Functional Group+−
Formula Weight+−
click to sign in and save
Methyl 2-(5,6-dimethoxy-1H-indazol-3-yl)acetate
click to sign in and save
Methyl 6-methoxy-1H-indazole-5-carboxylate
click to sign in and save
6-Methoxy-1H-indazole-5-carboxylic acid
* Country/Region
* Quantity Required :
* Cat. No.:
* CAS No :
* Product Name :
* Additional Information :