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There is a page named "2-Aminothiophenol" on Wikipedia
2-Aminothiophenol is an organosulfur compound with the formula C6H4(SH)(NH2). It is a colorless oily solid, although impure samples can be deeply colored...2 KB (119 words) - 13:41, 13 March 2024- Aminothiophenol may refer to: 2-Aminothiophenol 3-Aminothiophenol [Wikidata] 4-Aminothiophenol This set index article lists chemical compounds articles...439 bytes (45 words) - 16:50, 14 May 2022
Mercaptobenzothiazole (redirect from 2-mercaptobenzothiazole)+ S → C6H4(NH)SC=S + H2S The traditional route is the reaction of 2-aminothiophenol and carbon disulfide: C6H4(NH2)SH + CS2 → C6H4(NH)SC=S + H2S This...12 KB (1,134 words) - 13:47, 12 January 2024- converted to the 2-aminothiophenol. The 2-aminothiophenols are suitable for diazotization, giving benzothiadiazoles. Instead the sodium 2-aminothiophenolate...2 KB (242 words) - 14:45, 31 October 2023
- corresponding sodium thiolate, which can be further converted to the 2-aminothiophenol. Appel's salt is an example of a 1,2,3-dithiazolium. MacLean, Gregory...3 KB (318 words) - 03:42, 30 October 2023
3-Benzothiadiazole is readily prepared by the diazotisation reaction of 2-aminothiophenol or its disulfide with sodium nitrite, as originally reported in 1887...6 KB (594 words) - 09:39, 11 January 2024
Thioether formation between 2-Aminothiophenol (1) and 4-Chloro-N,N-Dimethyl-3-Nitrobenzenesulfonamide [137-47-3] (2) gives 4-(2-aminophenyl)sulfanyl-N...7 KB (474 words) - 12:45, 5 August 2024
Bernkop-Schnürch A (March 2010). "Hydrophobic thiolation of pectin with 4-aminothiophenol: synthesis and in vitro characterization". AAPS PharmSciTech. 11 (1):...39 KB (4,602 words) - 19:41, 14 July 2024
Chen-Guang (June 2018). "Redox-sensitive nanoparticles based on 4-aminothiophenol-carboxymethyl inulin conjugate for budesonide delivery in inflammatory...26 KB (3,054 words) - 08:01, 6 May 2024
- chloride, sulphuryl chloride, &c.; whilst ortho-phenylenediamine, o-aminophenol, and o-aminothiophenol give phenazine, phenoxazine and thiodiphenylamine.