6,6'-(E)-Diazene-1,2-diylbis(7H-purine), with the CAS number 26227-04-3, is a chemical compound characterized by its unique structure, which features two purine units linked by a diazene (N=N) moiety. This compound exhibits properties typical of purines, such as the ability to participate in hydrogen bonding and its role in biological systems, particularly in nucleic acid structures. The presence of the diazene linkage introduces potential reactivity, particularly in redox reactions, due to the double bond between the nitrogen atoms. Additionally, the compound may exhibit interesting optical properties and could be involved in various biochemical processes. Its solubility, stability, and reactivity can vary depending on the solvent and environmental conditions. As a purine derivative, it may also have implications in medicinal chemistry, particularly in the development of nucleoside analogs or other therapeutic agents. Overall, 6,6'-(E)-diazene-1,2-diylbis(7H-purine) represents a fascinating area of study within the field of organic and medicinal chemistry.

6,6'-(E)-diazene-1,2-diylbis(7H-purine)

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1H-Purine, 6,6'-azobis- (9CI)

6,6'-Azopurine is a hydrophobic organic compound that is used as an operational oxidant in the conversion of alcohols to aldehydes. It reacts with hydroxyl groups on the surface of the catalyst and undergoes nucleophilic attack to form a pyridinium salt. The reaction rate increases with increasing pH and temperature. 6,6'-Azopurine is also an immobilized oxidant that can be used for the oxidation of alcohols or hydrocarbons. Immobilization can be achieved by covalent coupling or adsorption on silica gel or alumina. 6,6'-Azopurine has been shown to have high activity against chlorides and is used for the oxidation of chlorides to produce chloride radicals.

CAS 26227-04-3: 6,6'-(E)-diazene-1,2-diylbis(7H-purine)

1H-Purine, 6,6'-azobis- (9CI)

Ref: IN-DA002SBY

6,6'-Azopurine

Ref: 3D-NA16207

6,6''-Azopurine

Ref: 7W-GN1764