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  2. Pyridinium perbromide - Wikipedia

    en.wikipedia.org/wiki/Pyridinium_perbromide

    Pyridinium perbromide (also called pyridinium bromide perbromide, pyridine hydrobromide perbromide, or pyridinium tribromide) is an organic chemical composed of a pyridinium cation and a tribromide anion. It can also be considered as a complex containing pyridinium bromide—the salt of pyridine and hydrogen bromide—with an added bromine (Br ...

  3. Pyridine - Wikipedia

    en.wikipedia.org/wiki/Pyridine

    Density: 0.9819 g/mL (20 ... and formation of the targeted substituted pyridine as well as pyridinium bromide. ... electron density in the ...

  4. Pyridinium - Wikipedia

    en.wikipedia.org/wiki/Pyridinium

    Pyridinium refers to the cation [C 5 H 5 NH] +. It is the conjugate acid of pyridine . Many related cations are known involving substituted pyridines, e.g. picolines, lutidines, collidines.

  5. Category:Bromides - Wikipedia

    en.wikipedia.org/wiki/Category:Bromides

    These may be metal salts containing bromide ion such as potassium bromide, or more covalent bromides of metals or nonmetals such as tantalum(V) bromide or phosphorus tribromide. See also [ edit ]

  6. Cornforth reagent - Wikipedia

    en.wikipedia.org/wiki/Cornforth_reagent

    The Cornforth reagent (pyridinium dichromate or PDC) is a pyridinium salt of dichromate with the chemical formula [C 5 H 5 NH] 2 [Cr 2 O 7].This compound is named after the Australian-British chemist Sir John Warcup Cornforth (b. 1917) who introduced it in 1962.

  7. Phosphorus tribromide - Wikipedia

    en.wikipedia.org/wiki/Phosphorus_tribromide

    The main use for phosphorus tribromide is for conversion of primary or secondary alcohols to alkyl bromides, [9] as described above.PBr 3 usually gives higher yields than hydrobromic acid, and it avoids problems of carbocation rearrangement- for example even neopentyl bromide can be made from the alcohol in 60% yield.

  8. Methylpyridinium - Wikipedia

    en.wikipedia.org/wiki/Methylpyridinium

    Methylpyridinium is prepared by treating pyridine with dimethylsulfate: [2]. C 5 H 5 N + (CH 3 O) 2 SO 2 → [C 5 H 5 NCH 3] + CH 3 OSO − 3. It is found in some coffee products. [3] It is not present in unroasted coffee beans, but is formed during roasting from its precursor chemical, trigonelline. [3]

  9. 4-Methylpyridine - Wikipedia

    en.wikipedia.org/wiki/4-Methylpyridine

    4-Methylpyridine is the organic compound with the formula CH 3 C 5 H 4 N. It is one of the three isomers of methylpyridine.This pungent liquid is a building block for the synthesis of other heterocyclic compounds.