Thiophenol is an organosulfur compound with the formula C6H5SH, sometimes abbreviated as PhSH. This foul-smelling colorless liquid is the simplest aromatic...
11 KB (992 words) - 00:26, 30 June 2024
The Leuckart thiophenol reaction is the decomposition of a diazoxanthate, by gentle warming in a slightly acidic cuprous medium, to its corresponding aryl...
2 KB (128 words) - 08:43, 13 August 2020
RLi + S → RSLi RSLi + HCl → RSH + LiCl Phenols can be converted to the thiophenols via rearrangement of their O-aryl dialkylthiocarbamates. Thiols are prepared...
35 KB (3,886 words) - 02:58, 4 July 2024
conversion is that often, it is the anion that is sought. More so than thiophenol, benzeneselenol is easily oxidized by air. The facility of this reaction...
5 KB (421 words) - 18:49, 27 January 2024
encountered organic disulfides in organic synthesis. Minor contamination by thiophenol is responsible for the disagreeable odour associated with this compound...
6 KB (472 words) - 21:04, 10 April 2024
250 ppm Safety data sheet (SDS) [1] Related compounds Related compounds Thiophenol Sodium phenoxide Except where otherwise noted, data are given for materials...
45 KB (4,802 words) - 20:23, 30 May 2024
Monofunctional compounds Methyl acetate Thiophenol Ethylamine...
5 KB (520 words) - 10:12, 24 June 2024
Suzuki reaction in a one-pot synthesis: DOM has also been used with thiophenols to prepare compounds that are useful as hindered ligands. Directed metallation...
9 KB (1,041 words) - 15:17, 1 February 2024
oxygen-centered ether—of anisole. It can be prepared by methylation of thiophenol. Alkyllithium reagents deprotonate thioanisole at the methyl group to...
3 KB (234 words) - 19:45, 27 October 2022
Newman–Kwart reaction represents a useful synthetic tool for the preparation of thiophenol derivatives. The Newman–Kwart rearrangement is intramolecular. It is generally...
6 KB (559 words) - 15:35, 5 March 2024