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2,4,6-Tribromoaniline Compound with spectra: 14 NMR, 4 FTIR, 1 Raman, and 8 MS (GC)
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Compound 2,5-Dibromoanilinewith free spectra: 5 NMR, 5 FTIR,...
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- 2,4,6-Tribromophenol
Compound 2,4,6-Tribromophenolwith free spectra: 5 NMR, 10...
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- 2,5-Dibromoaniline
The mutagenicity of 2,4,6-tribromoaniline was evaluated in Salmonella tester strains TA1535, TA1537, TA1538, TA98 and TA100 (Ames Test), and Saccharomyces cerevisiae strain D4, both in the presence and absence of metabolic activation by Aroclor-induced rat liver S9 fraction.
Aniline is the substrate. 2,4,6 tribromoaniline is the product on NMR test. Interpret the 1H-NMR for each product. Draw out the product and label each H unambiguously (i.e. label H’s a,b,c).
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% Standard InChI InChI=1S/C6H4Br3N/c7-3-1-4(8)6(10)5(9)2-3/h1-2H,10H2 Standard InChIKey GVPODVKBTHCGFU-UHFFFAOYSA-N
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.
2,4,6-Tribromoaniline View entire compound with spectra: 14 NMR, 4 FTIR, 1 Raman, and 8 MS (GC)
ChemSpider record containing structure, synonyms, properties, vendors and database links for 2,4,6-Tribromoaniline, 147-82-0.
