enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. 2,4,6-Tribromoaniline - Wikipedia

    en.wikipedia.org/wiki/2,4,6-tribromoaniline

    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. It is used in organic synthesis of pharmaceuticals, agrochemicals and fire-extinguishing agents.

  3. 1,3,5-Tribromobenzene - Wikipedia

    en.wikipedia.org/wiki/1,3,5-Tribromobenzene

    Brominating aniline with elemental bromine gives 2,4,6-tribromoaniline. This is then diazotized, then reacted with ethanol to replace the diazonium group with hydrogen, forming 1,3,5-tribromobenzene. [3] It has also been prepared by these methods: [3] replacement of the amino group of 3,5-dibromoaniline with bromine

  4. Bromoaniline - Wikipedia

    en.wikipedia.org/wiki/Bromoaniline

    The bromoanilines form a group of three isomers where the bromine atom occupies the para, ortho or meta position on the aromatic ring. Bromoaniline isomers Arene substitution patterns. The three isomers are: 2-Bromoaniline (o-Bromoaniline) [1] 3-Bromoaniline (m-Bromoaniline) [2] 4-Bromoaniline (p-Bromoaniline) [3]

  5. Tribromobenzene - Wikipedia

    en.wikipedia.org/wiki/Tribromobenzene

    Tribromobenzenes are a group of bromobenzenes with the formula C 6 H 3 Br 3, consisting of three bromine atoms bonded to a central benzene ring. There are three isomers of tribromobenzene: Tribromobenzene isomers

  6. 4-Bromoaniline - Wikipedia

    en.wikipedia.org/wiki/4-bromoaniline

    4-Bromoaniline is a compound where an aniline molecule is substituted with a bromine atom on the para position. Commercially available, this compound may be used as a building block, e.g. in the preparation of monobrominated biphenyl via the Gomberg-Bachmann reaction. [2]

  7. 2,4,6-Tribromophenol - Wikipedia

    en.wikipedia.org/wiki/2,4,6-Tribromophenol

    Microbial metabolism in products treated with TBP is known to produce 2,4,6-tribromoanisole (TBA), [9] which has a musty odor. In 2010 and 2011, Pfizer and Johnson & Johnson voluntarily recalled some products due to TBA odors from wooden pallets which were treated with TBP.

  8. Bismuth tribromide - Wikipedia

    en.wikipedia.org/wiki/Bismuth_tribromide

    Both polymorphs are monoclinic, but α-BiBr 3 is in space group P2 1 /a whereas β-BiBr 3 is in C2/m. α-BiBr 3 consists of pyramidal molecules whereas β-BiBr 3 is polymeric and adopts the AlCl 3 structure. BiBr 3 is the only group 15 trihalide that can adopt both molecular and polymeric structures. [3]

  9. Bromine compounds - Wikipedia

    en.wikipedia.org/wiki/Bromine_compounds

    Silver bromide (AgBr). Nearly all elements in the periodic table form binary bromides. The exceptions are decidedly in the minority and stem in each case from one of three causes: extreme inertness and reluctance to participate in chemical reactions (the noble gases, with the exception of xenon in the very unstable XeBr 2; extreme nuclear instability hampering chemical investigation before ...