Home Chemistry Heterocyclic Building Blocks Indazoles 6-Chloro-1H-Indazole
Substitution Reactions: The chlorine atom can undergo nucleophilic substitution reactions with various nucleophiles, leading to the formation of substituted indazoles.
Acylation: The nitrogen atom in the indazole ring can undergo acylation reactions to form N-acyl derivatives.
Reduction: The nitro group (if present) can be reduced to the corresponding amine using reducing agents such as iron and hydrochloric acid or tin and hydrochloric acid.
Cyclization Reactions: It can participate in cyclization reactions to form fused ring systems or other heterocyclic compounds.
Oxidation: It can undergo oxidation reactions to form various functionalized derivatives, such as oxides or ketones, under appropriate conditions.
Halogenation: It can undergo halogenation reactions, such as bromination or iodination, at other positions if suitable reagents are used.
Nucleophilic Addition: It can undergo nucleophilic addition reactions with suitable electrophiles, leading to the formation of addition products.
Metalation: It can undergo metalation reactions with organometallic reagents or metal amides to form organometallic complexes.
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Ethyl 6-chloro-1H-indazole-3-carboxylate
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6-Chloro-1H-indazole-5-carboxylic acid
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