Chemistry Heterocyclic Building Blocks Imidazoles 1-benzyl-1H-imidazole
Acylation and Alkylation Reactions: The nitrogen atom can act as a nucleophile and react with acylating or alkylating agents, forming amide or alkylated products, respectively.
Reduction: The imidazole ring might undergo reduction, especially under strong reducing conditions, leading to the formation of dihydroimidazoles.
Oxidation: Depending on the conditions, the compound might undergo oxidation reactions, leading to the formation of imidazole derivatives with additional oxygen-containing functional groups.
Base-Catalyzed Reactions: The imidazole ring is mildly basic. It can undergo reactions with strong acids, which may lead to protonation.
Metal Complexation: The nitrogen atoms in the imidazole ring can coordinate with metal ions, forming complexes.
Ring-Opening Reactions: Under certain conditions, the imidazole ring might open up to form linear or branched compounds.
Photolysis and Photoreactions: Exposure to light of specific wavelengths can lead to photochemical reactions.
Cross-Coupling Reactions: The benzyl group may participate in various cross-coupling reactions with appropriate coupling partners.
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2-((1H-Imidazol-1-yl)methyl)benzoic acid
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4-((1H-Imidazol-1-yl)methyl)benzoic acid
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Sodium 1-benzyl-1H-imidazole-2-carboxylate
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Methyl 1-(1-phenylethyl)-1H-imidazole-4-carboxylate
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Ethyl 4-amino-1-benzyl-1H-imidazole-5-carboxylate
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(3-((2-Isopropyl-1H-imidazol-1-yl)methyl)phenyl)amine dihydrochloride
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1-(4-Nitrobenzyl)-1H-imidazole(Chunks or pellets)