Home Chemistry Heterocyclic Building Blocks Indazoles Methyl 1H-Indazole-4-Carboxylate
Substitution Reactions: The carboxylate group can undergo nucleophilic substitution reactions with various electrophiles, leading to the formation of substituted esters.
Acid-Catalyzed Hydrolysis: The ester group can be hydrolyzed under acidic conditions to yield the corresponding carboxylic acid and alcohol.
Base-Catalyzed Hydrolysis: The ester group can undergo base-catalyzed hydrolysis to yield the corresponding carboxylic acid and alcohol.
Reduction: The carbonyl group of the ester can be reduced to the corresponding alcohol using reducing agents such as lithium aluminum hydride or sodium borohydride.
Oxidation: The alcohol group can be oxidized to the corresponding aldehyde or carboxylic acid under appropriate conditions.
Nucleophilic Addition: The ester group can undergo nucleophilic addition reactions with various nucleophiles to form addition products.
Decarboxylation: Under certain conditions, such as heating or treatment with specific reagents, decarboxylation may occur, leading to the loss of the carboxyl group.
Esterification: The alcohol group can react with carboxylic acids or acid derivatives to form esters through esterification reactions.
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Methyl 5-bromo-6-fluoro-1H-indazole-4-carboxylate
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Methyl 6-fluoro-1H-indazole-4-carboxylate
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Methyl 6-amino-1H-indazole-4-carboxylate
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Methyl 5-bromo-1H-indazole-4-carboxylate
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Methyl 6-chloro-1H-indazole-4-carboxylate
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