Home Chemistry Organic Building Blocks Ethers 1,2-Diphenoxyethane
Hydrolysis: The ether linkages in 1,2-diphenoxyethane can be hydrolyzed under acidic or basic conditions to form the corresponding alcohols and phenols.
Halogenation: 1,2-diphenoxyethane can undergo halogenation reactions, where halogens (e.g., chlorine, bromine) replace the hydrogen atoms in the molecule.
Esterification: 1,2-diphenoxyethane can undergo esterification reactions with acids to form esters.
Friedel-Crafts Acylation: The phenyl groups in 1,2-diphenoxyethane can undergo acylation reactions when treated with acylating agents in the presence of a Lewis acid catalyst, such as aluminum chloride (AlCl3). This can result in the introduction of an acyl group onto the phenyl rings.
Oxidation: The molecule can be oxidized under certain conditions to produce different oxidation products. For example, it can be oxidized to the corresponding ketone if exposed to an appropriate oxidizing agent.
Reduction: Under suitable conditions, 1,2-diphenoxyethane can undergo reduction reactions to convert functional groups like carbonyl groups or nitro groups to their respective reduced forms.
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1,1-(1,2-Ethanediylbis(oxy))bis(2,4,6-tribromobenzene)
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