2-chloro-6-methoxyphenol-Chlorides| Ambeed

Chemistry Heterocyclic Building Blocks Other Aromatic Heterocycles phenazine

phenazine

: Oxidation: Phenazine can be oxidized to form various compounds, such as phenazine-N-oxide or dioxophenazine. Oxidation can be achieved using oxidizing agents like hydrogen peroxide or potassium permanganate. Reduction: Phenazine can be reduced to produce dihydrophenazine or other reduced derivatives. This reduction can be accomplished using reducing agents like sodium borohydride or catalytic hydrogenation. Amination: Phenazine can undergo amination reactions to introduce amino groups. This can be achieved using ammonia or amine reagents. Halogenation: Phenazine can be halogenated by reacting with halogenating agents like chlorine or bromine, leading to the substitution of hydrogen atoms with halogen atoms. Alkylation and Acylation: Phenazine can be alkylated or acylated by reacting with alkyl or acyl halides in the presence of a base or a suitable catalyst. These reactions lead to the introduction of alkyl or acyl groups on the phenazine ring. Nucleophilic Substitution: Phenazine can undergo nucleophilic substitution reactions at appropriate positions. For example, reactions with nucleophiles like amines can lead to the substitution of hydrogen atoms with amino groups. Cyclization: Phenazine can undergo cyclization reactions to form various polycyclic compounds, depending on the reaction conditions and reagents used. Metal Complexation: Phenazine can form complexes with transition metals, and these complexes can have various applications in catalysis and materials chemistry.

phenazine

A34903169-48-795%

$245.00/1g

A375451553-24-2BS

$314.00/1kg

A2192012876-17-797%

$62.00/100mg

A17665592-82-097%

$12.00/25g

A115676436848-40-598%

$34.00/100mg

A146744550-89-098%

$23.00/100mg

A30140223462-25-195%

$1585.00/1g

A6001682876-22-495%

$85.00/1g

A161923655-86-790%

$17.00/1g