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  2. Category:Bromobenzenes - Wikipedia

    en.wikipedia.org/wiki/Category:Bromobenzenes

    If the benzene ring contains other substituents, it belongs in Category:Bromobenzene derivatives The main article for this category is Bromobenzenes . Pages in category "Bromobenzenes"

  3. Dibromobenzene - Wikipedia

    en.wikipedia.org/wiki/Dibromobenzene

    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 1.84 g/ml, solid Solubility in ...

  4. 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.

  5. Bromobenzene - Wikipedia

    en.wikipedia.org/wiki/Bromobenzene

    Bromobenzene is an aryl bromide and the simplest of the bromobenzenes, consisting of a benzene ring substituted with one bromine atom. Its chemical formula is C 6 H 5 Br . It is a colourless liquid although older samples can appear yellow.

  6. Bromobenzaldehyde - Wikipedia

    en.wikipedia.org/wiki/Bromobenzaldehyde

    Bromobenzaldehydes are any of three organic compounds with the formula BrC 6 H 4 COH, consisting of a formyl group and a bromine atom attached to a central benzene ring. They can be considered as brominated derivatives of benzaldehyde , or as formylated derivatives of bromobenzene .

  7. Bromochlorobenzene - Wikipedia

    en.wikipedia.org/wiki/Bromochlorobenzene

    1-Bromo-3-chlorobenzene: by (3-chlorophenyl)trimethylgermanium by electrophilic substitution [2] [better source needed] 1-Bromo-4-chlorobenzene: From a derivative of (4-bromophenyl)silane using N-bromosuccinimide [3] From 4-chlorophenol using triphenylphosphine dibromide [4] or phenylphosphorus tetrachloride [5]

  8. Benzyl bromide - Wikipedia

    en.wikipedia.org/wiki/Benzyl_bromide

    Benzyl bromide is used in organic synthesis for the introduction of the benzyl groups when the less expensive benzyl chloride is insufficiently reactive. [6] [7] Benzylations are often achieved in the presence of catalytic amounts of sodium iodide, which generates the more reactive benzyl iodide in situ. [3]

  9. Bromobenzenes - Wikipedia

    en.wikipedia.org/wiki/Bromobenzenes

    1,3-Dibromobenzene; 1,4-Dibromobenzene; Tribromobenzene. ... Below is an example reaction of 1,3-dibromobenzene to isophthalic acid. [1] See also. Fluorobenzenes;