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  2. Bromochlorobenzene - Wikipedia

    en.wikipedia.org/wiki/Bromochlorobenzene

    Isomers of Bromochlorobenzene Skeletal formula: General Common names o-bromochlorobenzene ortho-bromochlorobenzene m-bromochlorobenzene meta-bromochlorobenzene p-bromochlorobenzene para-bromochlorobenzene Systematic name: 1-bromo-2-chlorobenzene 1-bromo-3-chlorobenzene 1-bromo-4-chlorobenzene Molecular formula: BrC 6 H 4 Cl Molar mass: 191.45 g ...

  3. Bromotoluene - Wikipedia

    en.wikipedia.org/wiki/Bromotoluene

    Molecular formula: C 7 H 7 Br (C 6 H 4 BrCH 3) Molar mass: 171.03 g/mol Appearance colorless liquid colorless liquid white crystalline solid CAS number [95-46-5] [591-17-3] [106-38-7] Properties Density and phase: 1.431 g/ml, liquid 1.4099 g/ml, liquid 1.3995 g/ml, solid Solubility in water: practically insoluble Other solubilities

  4. 1-Bromo-4-fluorobenzene - Wikipedia

    en.wikipedia.org/wiki/1-Bromo-4-fluorobenzene

    4-Fluorobromobenzene is synthesized via bromination of fluorobenzene in the presence of a Lewis acid catalyst such as iron(III) bromide or aluminium tribromide. [2]4-Bromofluorobenzene is regarded by the Toxic Substances Control Act as a high production volume chemical, that is, a chemical that 1 million pounds (about 500 tonnes) per year is either produced in or imported to the United States.

  5. Bromobenzene - Wikipedia

    en.wikipedia.org/wiki/Bromobenzene

    Its chemical formula is C 6 H 5 Br. It is a colourless liquid although older samples can appear yellow. It is a colourless liquid although older samples can appear yellow. It is a reagent in organic synthesis .

  6. 1-Bromo-4-iodobenzene - Wikipedia

    en.wikipedia.org/wiki/1-bromo-4-iodobenzene

    Since aryl iodides are more reactive than aryl bromides in the Sonogashira coupling, [4] the iodine end of 1-bromo-4-iodobenzene can be selectively coupled to a terminal acetylene while leaving the bromine end unreacted, by running the reaction at room temperature.

  7. AL-1095 - Wikipedia

    en.wikipedia.org/wiki/AL-1095

    The conjugate addition of the Grignard reagent formed from 4-bromochlorobenzene [106-39-8] (4) to the enone gives the benzhydryl (5). MPV reduction of the carbonyl gives the syn stereoisomers, whereas borohydride gave trans.

  8. File:1-bromo-2-chlorobenzene 200.svg - Wikipedia

    en.wikipedia.org/wiki/File:1-bromo-2-chloro...

    This structural formula was created with Name2Struct - CS ChemDraw Ultra. The chemistry symbols of this structural formula are drawn using the path text method. The accuracy of this version of the structural formula has been verified as part of the Chemical Structure Validation project .

  9. Benzyl bromide - Wikipedia

    en.wikipedia.org/wiki/Benzyl_bromide

    Benzyl bromide is an organic compound with the formula C 6 H 5 CH 2 Br. The molecule consists of a benzene ring substituted with a bromomethyl group. It is a colorless liquid with lachrymatory properties. The compound is a reagent for introducing benzyl groups. [3] [4]