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Anderson also named picoline by combining the Latin words pix (tar) and oleum (oil) because coal tar oil was a source of picoline. [ 4 ] [ 5 ] By 1870, the German chemist Adolf von Baeyer had synthesized picoline in two ways: by the dry distillation of acroleïnammoniak (CH 2 =CH-CH=N-CHOH-CH=CH 2 ) [ 6 ] and by heating tribromallyl ( 1,2,3 ...
2-Methylpyridine, or 2-picoline, is the compound described with formula C 6 H 7 N. 2-Picoline is a colorless liquid that has an unpleasant odor similar to pyridine. It is mainly used to make vinylpyridine and the agrichemical nitrapyrin .
3-Methylpyridine or 3-picoline, is an organic compound with formula 3-CH 3 C 5 H 4 N. It is one of three positional isomers of methylpyridine, whose structures vary according to where the methyl group is attached around the pyridine ring. This colorless liquid is a precursor to pyridine derivatives that have applications in the pharmaceutical ...
Picolinic acid is an organic compound with the formula NC 5 H 4 CO 2 H.It is a derivative of pyridine with a carboxylic acid (COOH) substituent at the 2-position. It is an isomer of nicotinic acid and isonicotinic acid, which have the carboxyl side chain at the 3- and 4-positions, respectively.
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.
Chromium(III) picolinate (also trivalent chromium) is a chemical compound with the formula Cr(C 5 H 4 N(CO 2)) 3, commonly abbreviated as CrPic 3. It is a bright-red coordination compound derived from chromium(III) and picolinic acid.
Pyridine is a basic heterocyclic organic compound with the chemical formula C 5 H 5 N.It is structurally related to benzene, with one methine group (=CH−) replaced by a nitrogen atom (=N−).
Pyridine N-oxide is five orders of magnitude less basic than pyridine: the pK a of protonated pyridine-N-oxide is 0.8. [7] Protonated derivatives are isolable, e.g., [C 5 H 5 NOH]Cl. [3]