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2,4,6-Tribromoaniline Compound with spectra: 14 NMR, 4 FTIR, 1 Raman, and 8 MS (GC)
- 2,5-Dibromoaniline
Compound 2,5-Dibromoanilinewith free spectra: 5 NMR, 5 FTIR,...
- 2-Bromo-4-chloroaniline
Compound 2-Bromo-4-chloroanilinewith free spectra: 2 NMR, 5...
- 2,4,6-Tribromophenol
Compound 2,4,6-Tribromophenolwith free spectra: 5 NMR, 10...
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- 2,5-Dibromoaniline
The document describes the preparation of 2,4,6-tribromoaniline from aniline via electrophilic aromatic substitution. Aniline undergoes bromination at the ortho and para positions due to the activating effect of the amino group. This results in 2,4,6-tribromoaniline.
19 sie 2024 · 2, 4, 6-Tribromoaniline Principle. Aniline undergoes nucleophilic substitution with bromine, even in cold. The bromine atoms enter at the two ortho positions and the para position with the formation of 2,4,6-tribromoaniline.
3 lis 2019 · PRINCIPLE: Electrophilic aromatic substitution is an important class of organic chemistry. Substituents already present on benzene nucleus determine the position and extent of substitution of the new incoming groups.
2,4,6-Tribromoaniline is a brominated derivative of aniline with the formula C 6 H 4 Br 3 N. It is used in organic synthesis of pharmaceuticals, agrochemicals and fire-extinguishing agents. [1]
Monograph ID M11041 Title 2,4,6-Tribromoaniline UNII 0C2N8WIL3B Molecular formula C 6 H 4 Br 3 N Molecular weight 329.82 Percent composition C 21.85%, H 1.22%, Br 72.68%, N 4.25%
ChemSpider record containing structure, synonyms, properties, vendors and database links for 2,4,6-Tribromoaniline, 147-82-0.
