Home Chemistry Heterocyclic Building Blocks Indoles 1,2-Dimethyl-1H-Indole
Electrophilic Aromatic Substitution (EAS): Indoles are known to undergo electrophilic aromatic substitution reactions. The electron-rich nature of the Indole ring makes it susceptible to attack by electrophiles. This could include reactions with electrophiles such as halogens, nitration, sulfonation, or Friedel-Crafts acylation/alkylation.
Reduction: The Indole ring can be reduced under certain conditions. For instance, the double bond in the Indole ring may be reduced to a single bond, or other reductions might occur at the methyl groups.
Oxidation: Oxidation reactions may occur, affecting either the Indole ring or the methyl groups.
Alkylation: The methyl groups on the Indole ring can potentially undergo alkylation reactions under appropriate conditions.
Condensation Reactions: Depending on the reaction conditions and the presence of reactive functional groups, 1,2-dimethyl-1H-indole may participate in condensation reactions, such as Mannich reactions or 【Friedel-Crafts|https://www.ambeed.com/ti/nr/Friedel-Crafts-reaction.html】 reactions.
Substitution Reactions: The methyl groups and the hydrogen atoms on the indole ring can be subject to substitution reactions, depending on the reaction conditions and the nature of the substituents.
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5-Bromo-1,2-dimethyl-1H-indole-3-carboxylic acid
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