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  2. 2-Phenylethyl bromide - Wikipedia

    en.wikipedia.org/wiki/2-Phenylethyl_bromide

    2-Phenylethyl bromide is an organobromide with the formula C 6 H 5 CH 2 CH 2 Br. It is a colorless liquid, although older samples appear yellow. Analogous to the preparation of most 1-bromoalkanes, it is prepared by free-radical addition of hydrogen bromide to styrene. These conditions lead to anti-Markovnikov addition, giving the 1-bromo ...

  3. Organobromine chemistry - Wikipedia

    en.wikipedia.org/wiki/Organobromine_chemistry

    2-Phenethyl bromide (C 6 H 5 CH 2 CH 2 Br) is produced via this route from styrene. Hydrogen bromide can also be used to convert alcohols to alkyl bromides. This reaction, that must be done under low temperature conditions, is employed in the industrial synthesis of allyl bromide :

  4. Bromine compounds - Wikipedia

    en.wikipedia.org/wiki/Bromine_compounds

    Silver bromide (AgBr). Nearly all elements in the periodic table form binary bromides. The exceptions are decidedly in the minority and stem in each case from one of three causes: extreme inertness and reluctance to participate in chemical reactions (the noble gases, with the exception of xenon in the very unstable XeBr 2; extreme nuclear instability hampering chemical investigation before ...

  5. Bromide - Wikipedia

    en.wikipedia.org/wiki/Bromide

    Bromide salts are used in hot tubs as mild germicidal agents to generate in situ hypobromite. The bromide ion is antiepileptic and as bromide salt, is used in veterinary medicine in the US. The kidneys excrete bromide ions. The half-life of bromide in the human body (12 days) is long compared with many pharmaceuticals, making dosing challenging ...

  6. Phenyl group - Wikipedia

    en.wikipedia.org/wiki/Phenyl_group

    Phenyl radical group. In organic chemistry, the phenyl group, or phenyl ring, is a cyclic group of atoms with the formula C6H5, and is often represented by the symbol Ph (archaically φ) or Ø.

  7. Thiofentanyl - Wikipedia

    en.wikipedia.org/wiki/Thiofentanyl

    Thiofentanyl is made with the same synthetic route as fentanyl, but by substituting 2-(2-bromoethyl)thiophene for phenethyl bromide in the synthesis. Side effects of fentanyl analogs are similar to those of fentanyl itself, which include itching , nausea and potentially serious respiratory depression , which can be life-threatening.

  8. N-Phenethyl-4-piperidinone - Wikipedia

    en.wikipedia.org/wiki/N-Phenethyl-4-piperidinone

    N-Phenethyl-4-piperidinone (NPP) is a derivative of 4-piperidinone with the molecular formula C 13 H 17 NO. It is used as an intermediate in the manufacture of chemicals and pharmaceutical drugs such as fentanyl .

  9. Bromism - Wikipedia

    en.wikipedia.org/wiki/Bromism

    Bromide has an elimination half-life of 9 to 12 days, which can lead to excessive accumulation. Doses of 0.5 to 1 gram per day of bromide can lead to bromism. Historically, the therapeutic dose of bromide is about 3 to 5 grams of bromide, thus explaining why chronic toxicity (bromism) was once so common.