Home Chemistry Heterocyclic Building Blocks Imidazoles Imidazo[1,5-A]Pyrazine
Electrophilic Aromatic Substitution: Imidazo[1,5-a]pyrazine can undergo electrophilic aromatic substitution reactions, where an electrophile substitutes a hydrogen atom on the aromatic rings.
Nucleophilic Substitution: If there are suitable leaving groups attached to the imidazo[1,5-a]pyrazine, it can undergo nucleophilic substitution reactions.
Redox Reactions: Imidazo[1,5-a]pyrazine can participate in redox reactions, gaining or losing electrons to form reduced or oxidized products.
Ring-Opening Reactions: Ring-opening reactions can be carried out if the imidazo[1,5-a]pyrazine ring system contains functional groups that are prone to ring opening.
Cross-Coupling Reactions: Imidazo[1,5-a]pyrazine can be used as a substrate in cross-coupling reactions, such as Suzuki, Heck, or Stille reactions, to form new carbon-carbon or carbon-heteroatom bonds.
Halogenation: Imidazo[1,5-a]pyrazine can undergo halogenation reactions, where halogens like chlorine, bromine, or iodine can be introduced to the aromatic rings.
Oxidation and Reduction: It can be oxidized to form imidazo[1,5-a]pyrazine derivatives or reduced to yield dihydroimidazo[1,5-a]pyrazine derivatives.
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8-Chloro-1-iodo-3-isopropylimidazo[1,5-a]pyrazine
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6,8-Dichloro-3-methylimidazo[1,5-a]pyrazine
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8-Chloro-1-iodoimidazo[1,5-a]pyrazine
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Ethyl 8-chloroimidazo[1,5-a]pyrazine-1-carboxylate
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