Chemistry Organic Building Blocks Aryls 1,3-diphenylurea
Hydrolysis: 1,3-Diphenylurea can undergo hydrolysis when treated with an acid or a base, breaking the urea functional group. For example, under acidic conditions, it can yield phenyl isocyanate and phenylamine.
Substitution Reactions: You can perform substitution reactions on the phenyl groups of 1,3-diphenylurea. For instance, you can replace one or both of the phenyl groups with other functional groups or molecules. Common substitution reactions include nucleophilic aromatic substitution (SNAr) reactions.
Oxidation: Depending on the conditions, 1,3-diphenylurea can undergo oxidation, leading to various products. For example, the oxidation of ureas can produce isocyanates or other functional groups.
Reduction: Similarly, it can undergo reduction reactions, converting the urea functional group to other functional groups, such as primary amines.
Condensation Reactions: It can participate in condensation reactions with other compounds, leading to the formation of larger molecules.
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1,3-Bis(3,5-bis(trifluoromethyl)phenyl)urea
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1,3-Bis(4-chloro-3-(trifluoromethyl)phenyl)urea
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4,4'-(Carbonylbis(azanediyl))dibenzoic acid
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5,5'-(Carbonylbis(azanediyl))diisophthalic acid