Home Chemistry Organic Building Blocks Sulfides 1,2-Diphenyldisulfane
Nucleophilic Substitution: The sulfur atoms in the disulfide can undergo nucleophilic substitution reactions. For example, they can react with strong nucleophiles (e.g., sodium or potassium hydride) to form the corresponding thiol compounds.
Oxidation: Diphenyl disulfide can be oxidized to form diphenyl sulfone by the action of strong oxidizing agents like hydrogen peroxide (H2O2).
Reduction: It can be reduced to the corresponding thiol, such as diphenyl sulfide, using reducing agents like sodium borohydride (NaBH4) or dithionite.
Disulfide Exchange: Diphenyl disulfide can undergo disulfide exchange reactions with other disulfides or thiol compounds. For instance, it can react with thiols to form mixed disulfides or with other disulfides to exchange sulfur atoms.
Halogenation: The aromatic rings in diphenyl disulfide can undergo halogenation reactions, such as chlorination or bromination, under appropriate conditions.
Cross-Coupling Reactions: Diphenyl disulfide can be used in cross-coupling reactions, such as the Ullmann coupling, where it reacts with an aryl halide in the presence of a metal catalyst to form a new carbon-carbon bond.
Acid-Catalyzed Reactions: Under acidic conditions, diphenyl disulfide can undergo reactions like hydrolysis, leading to the formation of thiols and other products.
Framework+−
By Key Group+−
By Parent Nucleus+−
By Functional Group+−
Sulfur related+−
Formula Weight+−
* Country/Region
* Quantity Required :
* Cat. No.:
* CAS No :
* Product Name :
* Additional Information :