2-amino-2-phenylethan-1-ol-Alcohols| Ambeed

Chemistry Heterocyclic Building Blocks Quinoxalines 1,2,3,4-tetrahydroquinoxaline

1,2,3,4-tetrahydroquinoxaline

: Amination: 1,2,3,4-Tetrahydroquinoxaline can be mono- or poly-aminated, introducing amino groups into the molecule. This can be achieved by using various aminating agents, such as ammonia or amine reagents. Halogenation: You can brominate or chlorinate 1,2,3,4-tetrahydroquinoxaline by using halogenating agents like bromine or chlorine in the presence of a suitable catalyst. Hydrogenation: The double bonds in the quinoxaline ring can be reduced to saturated bonds by using hydrogen gas in the presence of a suitable catalyst (e.g., palladium on carbon). This would convert the compound into a tetrahydroquinoxaline. Oxidation: You can oxidize 1,2,3,4-tetrahydroquinoxaline to form various oxidation products using oxidizing agents like potassium permanganate (KMnO₄) or hydrogen peroxide (H₂O2). Ring-Opening Reactions: If there are suitable functional groups in the molecule, you can perform ring-opening reactions to open the quinoxaline ring and form new compounds. For example, nucleophilic ring-opening reactions with strong bases can be used to open the ring. Substitution Reactions: Depending on the substituents on the tetrahydroquinoxaline ring, you can perform various substitution reactions. For example, if there are halogen atoms on the ring, nucleophilic substitutions or elimination reactions can be carried out. Cyclization: Depending on the reaction conditions and reagents, you can induce intramolecular cyclization reactions within the molecule to form different cyclic compounds.

1,2,3,4-tetrahydroquinoxaline

A11267013311-79-097%

$45.00/100mg

A255139912284-82-395%

$60.00/250mg

A22875413311-77-897%

$23.00/100mg

A1287693476-89-997%

$25.00/10g

A11409556640-55-798%

$465.00/5g

A29314341959-35-798%

$64.00/1g