enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Bromophenol - Wikipedia

    en.wikipedia.org/wiki/Bromophenol

    Chemical structure of 2-bromophenol. A bromophenol is an organic compound consisting of hydroxyl groups and bromine atoms bonded to a benzene ring. They may be viewed as hydroxyl derivatives of bromobenzene, or as brominated derivatives of phenol.

  3. Monobromophenol - Wikipedia

    en.wikipedia.org/wiki/Monobromophenol

    2-Bromophenol: 3-Bromophenol: 4-Bromophenol: Other names o-Bromophenol: m-Bromophenol: p-Bromophenol Chemical structure: CAS number: 95-56-7: 591-20-8: 106-41-2 PubChem ID CID 7244 from PubChem: CID 11563 from PubChem: CID 7808 from PubChem: Chemical formula: C 6 H 5 BrO Molar mass: 173.02 g/mol 1: Physical state: liquid solid Melting point: 3 ...

  4. Dibromophenol - Wikipedia

    en.wikipedia.org/wiki/Dibromophenol

    There are six structural isomers, each with the molecular formula C 6 H 4 Br 2 O, which differ by arrangement of the substituents. Dibromophenols: Name 2,3-Dibromophenol,

  5. 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. [10] [11] [12] [13]

  6. Dibromobenzene - Wikipedia

    en.wikipedia.org/wiki/Dibromobenzene

    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 ...

  7. 4-Bromothiophenol - Wikipedia

    en.wikipedia.org/wiki/4-bromothiophenol

    It reacts with acetylacetone in the presence of cesium carbonate to give 3-(4-bromophenylthio)pentane-2,4-dione. 4,4'-Dibromophenyl disulfide is also produced as the intermediate. [5] Like other thiols, it reacts with silver nitrate to produce silver 4-bromothiophenolate. [6]

  8. Xylenol - Wikipedia

    en.wikipedia.org/wiki/Xylenol

    The main xylenols in such tar are the 3,5-, 2,4, and 2,3- isomers. 2,6-Xylenol is produced by methylation of phenol using methanol in the presence of metal oxide catalysts: [1] C 6 H 5 OH + 2 CH 3 OH → (CH 3) 2 C 6 H 3 OH + 2 H 2 O. Typically, xylenols also ethylphenols, which have very similar physical properties. [2]

  9. 2,4-Dibromophenol - Wikipedia

    en.wikipedia.org/wiki/2,4-Dibromophenol

    At room temperature, 2,4-dibromophenol is a solid with needle-like crystals. It melts at 38 °C (100.4 °F) and boils at 238.5 °C (461.3 °F). it has a molecular weight of 251.905 g/mol. It is soluble in water, ethanol, ether and benzene and slightly soluble in carbon tetrachloride. [1]