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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

    Free-radical addition is used commercially for the synthesis of 1-bromoalkanes, precursors to tertiary amines and quaternary ammonium salts. 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.

  4. Phenethyl alcohol - Wikipedia

    en.wikipedia.org/wiki/Phenethyl_alcohol

    Phenethyl alcohol can also be prepared by the reaction between phenylmagnesium bromide and ethylene oxide: C 6 H 5 MgBr + (CH 2 CH 2)O → C 6 H 5 CH 2 CH 2 OMgBr C 6 H 5 CH 2 CH 2 OMgBr + H + → C 6 H 5 CH 2 CH 2 OH + MgBr + Phenethyl alcohol can also be produced by biotransformation from L-phenylalanine using immobilized yeast Saccharomyces ...

  5. 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 .

  6. 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 ...

  7. Trifluoromethylation - Wikipedia

    en.wikipedia.org/wiki/Trifluoromethylation

    Trifluoromethanesulfonyl chloride (or triflyl chloride, CF3SO2Cl) can be used in a highly efficient method to introduce a trifluoromethyl group to aromatic and heteroaromatic systems, including known pharmaceuticals such as Lipitor. The chemistry is general and mild, and uses a photoredox catalyst and a light source at room temperature. [27]

  8. DEA list of chemicals - Wikipedia

    en.wikipedia.org/wiki/DEA_list_of_chemicals

    Organomagnesium halides (Grignard reagents) (e.g. ethylmagnesium bromide and phenylmagnesium bromide) phencyclidine ortho-Toluidine: methaqualone: 2-Phenylethyl bromide: fentanyl: Phenylethanolamine and its salts Phosphorus pentachloride: lysergic acid diethylamide Potassium dichromate: general-purpose oxidizing agent Pyridine and its salts

  9. Category:Phenyl compounds - Wikipedia

    en.wikipedia.org/wiki/Category:Phenyl_compounds

    B. Bavdegalutamide; Benzal chloride; Benzaldehyde; Benzamide; Benzamidine; Benzathine; Benzenediazonium tetrafluoroborate; Benzeneselenol; Benzenesulfonic acid