Home Chemistry Heterocyclic Building Blocks Pyrazines [1,2,4]Triazolo[4,3-A]Pyrazine
Nucleophilic Substitution: The nitrogen atoms in the triazole and pyrazine rings can act as nucleophilic centers, and the compound can undergo nucleophilic substitution reactions with electrophiles.
Electrophilic Aromatic Substitution: If there are electron-rich substituents on the aromatic rings, [1,2,4]triazolo[4,3-a]pyrazine can undergo electrophilic aromatic substitution reactions, such as nitration, halogenation, or sulfonation.
Alkylation and Acylation: The nitrogen atoms in the heterocyclic rings can be alkylated or acylated using appropriate alkylating or acylating agents.
Redox Reactions: [1,2,4]triazolo[4,3-a]pyrazine can participate in redox reactions, such as oxidation or reduction, depending on the reaction conditions and reagents used.
Cross-Coupling Reactions: It can participate in various cross-coupling reactions with appropriate reagents, leading to the formation of new carbon-carbon or carbon-heteroatom bonds.
Cyclization Reactions: [1,2,4]triazolo[4,3-a]pyrazine can undergo cyclization reactions to form larger, more complex heterocyclic compounds.
Framework+−
By Key Group+−
By Parent Nucleus+−
By Functional Group+−
Heterocyclic related+−
Formula Weight+−
click to sign in and save
6-Bromo-8-methoxy-[1,2,4]triazolo[4,3-a]pyrazine
click to sign in and save
6-Bromo-8-chloro-3-methyl-[1,2,4]triazolo[4,3-a]pyrazine
click to sign in and save
8-Chloro-3-methyl-[1,2,4]triazolo[4,3-a]pyrazine
click to sign in and save
6-Bromo-[1,2,4]triazolo[4,3-a]pyrazine
click to sign in and save
Ethyl 1,2,4-Triazolo[4,3-a]pyrazine-3-carboxylate
* Country/Region
* Quantity Required :
* Cat. No.:
* CAS No :
* Product Name :
* Additional Information :