Thiophenol is an organosulfur compound with the formula C6H5SH, sometimes abbreviated as PhSH. This foul-smelling colorless liquid is the simplest aromatic...

The Leuckart thiophenol reaction is the decomposition of a diazoxanthate, by gentle warming in a slightly acidic cuprous medium, to its corresponding aryl...

RLi + S → RSLi RSLi + HCl → RSH + LiCl Phenols can be converted to the thiophenols via rearrangement of their O-aryl dialkylthiocarbamates. Thiols are prepared...

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...

encountered organic disulfides in organic synthesis. Minor contamination by thiophenol is responsible for the disagreeable odour associated with this compound...

250 ppm Safety data sheet (SDS) [1] Related compounds Related compounds Thiophenol Sodium phenoxide Except where otherwise noted, data are given for materials...

Monofunctional compounds Methyl acetate Thiophenol Ethylamine...

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...

oxygen-centered ether—of anisole. It can be prepared by methylation of thiophenol. Alkyllithium reagents deprotonate thioanisole at the methyl group to...

Newman–Kwart reaction represents a useful synthetic tool for the preparation of thiophenol derivatives. The Newman–Kwart rearrangement is intramolecular. It is generally...