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Tribromobenzene isomers Common name and systematic name 1,2,3-Tribromobenzene [1] [2] 1,2,4-Tribromobenzene [3] [4] 1,3,5-Tribromobenzene [5] [6] Structure Molecular formula: C 6 H 3 Br 3: Molar mass: 314.802 g/mol Appearance colorless solid CAS number [608-21-9] [615-54-3] [626-39-1] Properties Solubility in water: practically insoluble ...
1,3,5-Tribromobenzene is a precursor to C 3-symmetric molecules. It undergoes a Suzuki reaction with three equivalents of 4-formylphenylboronic acid to form 1,3,5-tris(4-formylphenyl)benzene (TFPB), a monomer for covalent organic frameworks .
Diazotization, then reaction with ethanol to replace the diazonium group with hydrogen, gives 1,3,5-tribromobenzene. [2] See also. Bromine test; 4-Bromoaniline;
tribromobenzene: C 6 H 3 F 7 O 2: vinyl perfluoro butyrate: 356-28-5 C 6 H 3 O 5 Re: methyl rhenium pentacarbonyl: 14524-92-6 C 6 H 4: benzyne: 462-80-6 C 6 H 4 Br 2: dibromobenzene: C 6 H 4 BrCl 3 Si: bromophenyltrichlorosilane: 27752-77-8 C 6 H 4 BrI: 1-Bromo-4-iodobenzene: 589-87-7 C 6 H 4 F 6 O 2: hexafluoroisopropyl acrylate: 2160-89-6 C 6 ...
Bromobenzene is prepared by the action of bromine on benzene in the presence of Lewis acid catalysts such as aluminium chloride or ferric bromide. [3]Bromobenzene is used to introduce a phenyl group into other compounds.
1,3,5-Tribromobenzene This page was last edited on 1 February 2024, at 18:49 (UTC). Text is available under the Creative Commons Attribution-ShareAlike 4.0 ...
Bromobenzenes may be carboxylated into carboxylic acids using carbon monoxide.The reaction takes place in a two-phase mixture of p-xylene and water as solvent, in the presence of catalytic PdCl
The original halogen dance is the base-catalysed rearrangement of 1,2,4-tribromobenzene to 1,3,5-tribromobenzene in liquid ammonia with the aniline/potassium base system. The intermediate in this reaction is an aryl carbanion.