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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. IUPAC nomenclature of organic chemistry - Wikipedia

    en.wikipedia.org/wiki/IUPAC_nomenclature_of...

    The alkyl (R') group is named first. The R−C(=O)O part is then named as a separate word based on the carboxylic acid name, with the ending changed from "-oic acid" to "-oate" or "-carboxylate" For example, CH 3 CH 2 CH 2 CH 2 COOCH 3 is methyl pentanoate, and (CH 3) 2 CHCH 2 CH 2 COOCH 2 CH 3 is ethyl 4-methylpentanoate.

  4. Dibromophenol - Wikipedia

    en.wikipedia.org/wiki/Dibromophenol

    3,5-Dibromophenol, 1,3-Dibromo-5-hydroxybenzene Structural formula: CAS Number: 57383-80-9: 615-58-7: 28165-52-8: 608-33-3: 615-56-5: 626-41-5 PubChem: CID 34264 from PubChem: CID 12005 from PubChem: CID 34177 from PubChem: CID 11847 from PubChem: CID 12003 from PubChem: CID 12280 from PubChem: Chemical formula: C 6 H 4 Br 2 O Molar mass: 251. ...

  5. 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.

  6. 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.

  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. DBDMH - Wikipedia

    en.wikipedia.org/wiki/DBDMH

    DBDMH (also known as 1,3-Dibromo-5,5-Dimethylhydantoin) is an organic compound derived from the heterocycle called dimethylhydantoin.This white crystalline compound with a slight bromine odor is widely used as a disinfectant used for drinking water purification, recreational water treatment, as a bleaching agent in pulp and paper mills, and for treating industrial/commercial water cooling systems.

  9. Dibromobenzene - Wikipedia

    en.wikipedia.org/wiki/Dibromobenzene

    Common name and systematic name 1,2-Dibromobenzene: 1,3-Dibromobenzene [1] 1,4-Dibromobenzene [2] [3] [4] Structure Molecular formula: C 6 H 4 Br 2: Molar mass: 235.906 g/mol Appearance colorless liquid colorless liquid white solid CAS number [583-53-9] [108-36-1] [106-37-6] Properties Density and phase: 1.9940 g/ml, liquid 1.9523 g/ml, liquid ...