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  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. There are five basic types of bromophenols (mono- to pentabromophenol) and 19 different ...

  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. File:4-Bromophenol.svg - Wikipedia

    en.wikipedia.org/wiki/File:4-Bromophenol.svg

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  5. 2,4,6-Tribromophenol - Wikipedia

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

    2,4,6-Tribromophenol (TBP) is a brominated derivative of phenol. It is used as a fungicide, as a wood preservative, and an intermediate in the preparation of flame ...

  6. 4-Bromothiophenol - Wikipedia

    en.wikipedia.org/wiki/4-bromothiophenol

    4-Bromothiophenol is an organic compound with the formula BrC 6 H 4 SH. It forms colorless crystals. Synthesis. 4-Bromothiophenol can be synthesized via the ...

  7. 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,

  8. 3-bromophenol - Wikipedia

    en.wikipedia.org/?title=3-bromophenol&redirect=no

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  9. 4-Bromophenylacetic acid - Wikipedia

    en.wikipedia.org/wiki/4-Bromophenylacetic_acid

    4-Bromophenylacetic acid may be prepared by the addition of a bromine atom to phenylacetic acid through electrophilic aromatic substitution.It was first prepared in the laboratory by treatment of phenylacetic acid with bromine and mercuric oxide; a mixture of the 2- and 4- isomers is made, and the 4- isomer is isolated by fractional crystallization.