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  2. Tetrabromobisphenol A diglycidyl ether - Wikipedia

    en.wikipedia.org/wiki/Tetrabromobisphenol_A...

    This species is then further reacted with sodium hydroxide to form the diglycidyl ether. [5] Higher molecular weight epoxy resins with bromine atoms along the chain maybe synthesized by reacting standard epoxy resin with tetrabromobisphenol A in a technique called advancement.

  3. Cyclohexane-1,2,3,4,5,6-hexol - Wikipedia

    en.wikipedia.org/wiki/Cyclohexane-1,2,3,4,5,6-hexol

    Cyclohexane-1,2,3,4,5,6-hexol is a family of chemical compounds with formula C 6 H 12 O 6, whose molecule consists of a ring of six carbon atoms, each bound to one hydrogen atom and one hydroxyl group (–OH). There are nine stereoisomers, that differ by the position of the hydroxyl groups relative to the mean plane of the ring.

  4. Category:Hexanols - Wikipedia

    en.wikipedia.org/wiki/Category:Hexanols

    Hexanol may refer to any isomeric organic compounds with the formula C 6 H 13 OH: Pages in category "Hexanols" The following 17 pages are in this category, out of 17 total.

  5. 5,6-Dibromo-N-methyltryptamine - Wikipedia

    en.wikipedia.org/wiki/5,6-Dibromo-N-methyltryptamine

    This page was last edited on 25 January 2023, at 23:31 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.

  6. 5-Bromo-DMT - Wikipedia

    en.wikipedia.org/wiki/5-Bromo-DMT

    5-Bromo-DMT (5-bromo-N,N-dimethyltryptamine) is a psychedelic brominated indole alkaloid found in the sponges Smenospongia aurea and Smenospongia echina, as well as in Verongula rigida (0.00142% dry weight) alongside 5,6-Dibromo-DMT (0.35% dry weight) and seven other alkaloids.

  7. Dibromomethane - Wikipedia

    en.wikipedia.org/wiki/Dibromomethane

    Dibromomethane is used as a solvent, gauge fluid, and in organic synthesis (often as 1 H-NMR internal standard). [3] It conviently converts polyols (such as catechols) to their methylenedioxy derivatives, and bromomethylenates enolates. It is a much cheaper precursor to a Simmons-Smith-type reagent than diiodomethane. [5]

  8. Bromoform - Wikipedia

    en.wikipedia.org/wiki/Bromoform

    Bromoform was discovered in 1832 by Löwig who distilled a mixture of bromal and potassium hydroxide, as analogous to preparation of chloroform from chloral. [5]Bromoform can be prepared by the haloform reaction using acetone and sodium hypobromite, by the electrolysis of potassium bromide in ethanol, or by treating chloroform with aluminium bromide.

  9. Epoxy - Wikipedia

    en.wikipedia.org/wiki/Epoxy

    The tetrabrominated bisphenol A (TBBPA, 2,2-bis(3,5-dibromophenyl)propane) or its diglycidyl ether, 2,2-bis[3,5-dibromo-4-(2,3-epoxypropoxy)phenyl]propane, can be added to the epoxy formulation. The formulation may then be reacted in the same way as pure bisphenol A.

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