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  2. Phenacyl bromide - Wikipedia

    en.wikipedia.org/wiki/Phenacyl_bromide

    Phenacyl bromide is the organic compound with the formula C 6 H 5 C(O)CH 2 Br. This colourless solid is a powerful lachrymator as well as a useful precursor to other organic compounds. It is prepared by bromination of acetophenone: [2] C 6 H 5 C(O)CH 3 + Br 2 → C 6 H 5 C(O)CH 2 Br + HBr. The compound was first reported in 1871. [3]

  3. Phenacyl group - Wikipedia

    en.wikipedia.org/wiki/Phenacyl_group

    In organic chemistry, a phenacyl group is an aromatic substituent that consists of a phenyl group attached to an acyl group. A molecule containing a phenacyl group has the formula RCH 2 (CO)C 6 H 5 and the structure shown to the right. Here, R denotes the remainder of the molecule; for instance, if R is Br, then the compound could be called ...

  4. 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.

  5. Bromoacetone - Wikipedia

    en.wikipedia.org/wiki/Bromoacetone

    Bromoacetone is available commercially, sometimes stabilized with magnesium oxide.It was first described in the 19th century, attributed to N. Sokolowsky. [3]Acetone and bromine form bromoacetone.

  6. Monobromophenol - Wikipedia

    en.wikipedia.org/wiki/Monobromophenol

    English. Read; Edit; View history; Tools. Tools. move to sidebar hide. Actions Read; ... CAS number: 95-56-7: 591-20-8: 106-41-2 PubChem ID CID 7244 from PubChem: CID ...

  7. Phenylacetylene - Wikipedia

    en.wikipedia.org/wiki/Phenylacetylene

    In the laboratory, phenylacetylene can be prepared by elimination of hydrogen bromide from styrene dibromide using sodium amide in ammonia: [3]. It can also be prepared by the elimination of hydrogen bromide from bromostyrene using molten potassium hydroxide. [4]

  8. File:Phenacyl bromide.svg - Wikipedia

    en.wikipedia.org/wiki/File:Phenacyl_bromide.svg

    English: Structure of phenacyl bromide; 2-Bromo-1-phenylethanone; 2-Bromoacetophenone; omega-Bromoacetophenone; Bromomethyl phenyl ketone Deutsch: ω-Bromacetophenon; Phenacylbromid; 2-Bromacetophenon

  9. Chloroacetyl chloride - Wikipedia

    en.wikipedia.org/wiki/Chloroacetyl_chloride

    Some chloroacetyl chloride is also used to produce phenacyl chloride, another chemical intermediate, also used as a tear gas. [3] Phenacyl chloride is synthesized in a Friedel-Crafts acylation of benzene, with an aluminium chloride catalyst: [6] With anisole, it is used for the synthesis of venlafaxine.

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