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2-Bromopyridine reacts with butyllithium to give 2-lithiopyridine, [2] which is a versatile reagent. [3] Pyrithione can be prepared in a two-step synthesis from 2-bromopyridine by oxidation to the N-oxide with a suitable peracid followed by substitution using either sodium dithionite or sodium sulfide with sodium hydroxide to introduce the thiol functional group.
2-Aminopyridine is an organic compound with the formula H 2 NC 5 H 4 N. It is one of three isomeric aminopyridines. It is a colourless solid that is used in the production of the drugs piroxicam, sulfapyridine, tenoxicam, and tripelennamine. It is produced by the reaction of sodium amide with pyridine, the Chichibabin reaction. [3]
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−). It is a highly flammable, weakly alkaline, water-miscible liquid with a distinctive, unpleasant fish-like smell.
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] [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-tribromopropane) with ammonia in ethanol. [7] In 1871, the English chemist and physicist James Dewar speculated that picoline was ...
A pyridinecarboxylic acid is any member of a group of organic compounds which are monocarboxylic derivatives of pyridine. Pyridinecarboxylic acid comes in three isomers: Picolinic acid (2-pyridinecarboxylic acid) Nicotinic acid (3-pyridinecarboxylic acid), also known as Niacin; Isonicotinic acid (4-pyridinecarboxylic acid)
Chemical formula. C 5 H 6 N 2: Molar mass: 94.117 g·mol −1 Appearance [citation needed] ... [2] It can be used in the synthesis of organic ligand 3 ...
C 2 H 5 Br: bromoethane: 74-96-4 C 2 H 5 NH 2: ethylamine: 75-04-7 C 2 H 5 NO 2: glycine Gly: 56-40-6 C 2 H 5 O −: ethoxide ion: C 2 H 5 OH: ethanol ethyl alcohol: 64-17-5 (C 2 H 5) 2 NH: diethylamine: 109-89-7 C 2 H 5 OCs: caesium ethoxide: C 2 H 5 OK: potassium ethoxide: 917-58-8 C 2 H 5 ONa: sodium ethoxide: 141-52-6 C 2 H 5 ORb: rubidium ...