Thiophenol - Wikipedia
WEBThiophenol is an organosulfur compound with the formula C 6 H 5 SH, sometimes abbreviated as PhSH. This foul-smelling colorless liquid is the simplest aromatic thiol. The chemical structures of thiophenol and its derivatives are analogous to phenols.
Thiophenol 97 108-98-5 - MilliporeSigma
WEBAldrich-T32808; Thiophenol 0.97; CAS No.: 108-98-5; Synonyms: Benzenethiol; Phenyl mercaptan; Linear Formula: C6H5SH; Empirical Formula: C6H6S; find related products, papers, technical documents, MSDS & more at Sigma-Aldrich.
Benzenethiol - NIST Chemistry WebBook
WEBFormula: C 6 H 6 S. Molecular weight: 110.177. IUPAC Standard InChI: InChI=1S/C6H6S/c7-6-4-2-1-3-5-6/h1-5,7H. IUPAC Standard InChIKey: RMVRSNDYEFQCLF-UHFFFAOYSA-N. CAS Registry Number: 108-98-5. Chemical structure: This structure is also available as a 2d Mol file or as a computed 3d SD file. The 3d structure may be viewed using Java or Javascript.
Thiophenol | C6H6S - ChemSpider
WEBThiophenol. Molecular formula: C 6 H 6 S. Average mass: 110.174. Monoisotopic mass: 110.019021. ChemSpider ID: 7681.
Organosulfur compound - Thiols, Structure, Reactions
WEBSimilar to alcohols, thiols react with alkalies and other bases to form salts. In the presence of heavy metal salts (such as those of mercury, lead, silver, or copper), thiols form mercaptides (metal thiolates), which are insoluble in water but are frequently soluble in organic solvents.
Thiophenol - an overview | ScienceDirect Topics
WEBAs synthetic raw materials and intermediates, thiophenols are widely involved in various aeras, such as pesticides, medicines and industrial products. However, thiophenols are also highly toxic species that cause irreversible damage to the central nervous system with long-term exposure in either liquid or vapor conditions [77, 78].
Thiophenol - an overview | ScienceDirect Topics
WEBTreatment of a thiophenol /β-keto ester mixture with an acid represents a conventional way to produce thiochromones.
Thiophenol - chemeurope.com
WEBThiophenol is a chemical compound with the formula C 6 H 5 SH, and sometimes abbreviated as PhSH. The foul-smelling liquid is the principal aromatic thiol.
Thiol - Wikipedia
WEBIn organic chemistry, a thiol (/ ˈθaɪɒl /; [1] from Ancient Greek θεῖον (theion) ' sulfur ' [2]), or thiol derivative, is any organosulfur compound of the form R−SH, where R represents an alkyl or other organic substituent. The −SH functional group itself is referred to as either a thiol group or a sulfhydryl group, or a sulfanyl group.
Thiophenol - an overview | ScienceDirect Topics
WEB2.5.1 Introduction. Three different types of thiocarboxylic esters (and also thiolactones) exist: the thiol, thioxo- and dithioesters which, according to the IUPAC rules, are named S -alkyl (S -aryl) carbothioates (1), O -alkyl l (O -aryl) carbothioates (2) or alkyl (aryl) carbodithioates (3).
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