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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.
Pyrithione is the common name of an organosulfur compound with molecular formula C 5 H 5 NOS, chosen as an abbreviation of pyridinethione, and found in the Persian shallot. [4] It exists as a pair of tautomers, the major form being the thione 1-hydroxy-2(1H)-pyridinethione and the minor form being the thiol 2-mercaptopyridine N-oxide; it crystallises in the thione form. [5]
Patients can sometimes arrive at hospital by ambulance without footwear, and are typically provided with socks having a rubberised tread pattern to improve their grip strength. These non-slip socks are intended as alternative footwear to help prevent falls, but there is limited evidence for their usefulness. [2]
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Counterirritant patches are sold over-the-counter and do not require a prescription. Other over-the-counter products marketed for the relief of minor injury or arthritis pain include Absorbine Jr. Pain Relief, Excedrin Cooling Pads, and Icy Hot Patches. [4] In Japan, Salonpas, produced by Hisamitsu Pharmaceutical, remains a popular brand. Other ...
2-Mercaptopyridine was originally synthesized in 1931 by heating 2-chloropyridine with calcium hydrogen sulfide. [2]ClC 5 H 4 N + Ca(SH) 2 → HSC 5 H 4 N + Ca(SH)Cl. A more convenient route to 2-mercaptopyridine is the reaction of 2-chloropyridine and thiourea in ethanol and aqueous ammonia.
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2,2′-Dipyridyldisulfide, sometimes known as DPS, is used for preparing thiols [1] [2] and activating carboxylic acid for coupling reactions, as in the following reaction: [3] Uses [ edit ]