2-Aminothiophenol was used in the synthesis of 1,5-benzothiazepines derivatives by reacting with 1,3-diphenylpropenone derivatives and using aluminosilicate solid catalysts. It was also used in the synthesis of benzothiazole2 and 3-(benzothiazol-2-yl)coumarin derivatives. The ternary complexes of copper (II) with salicylidene-2-aminothiophenol (L) and glycine, alanine, valine and histidene amino acids.
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Applications
2-Aminothiophenol was used in the synthesis of 1,5-benzothiazepines derivatives by reacting with 1,3-diphenylpropenone derivatives and using aluminosilicate solid catalysts. It was also used in the synthesis of benzothiazole2 and 3-(benzothiazol-2-yl)coumarin derivatives. The ternary complexes of copper (II) with salicylidene-2-aminothiophenol (L) and glycine, alanine, valine and histidene amino acids.
Solubility
Insoluble in water.
Notes
Air Sensitive. Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Store away from strong oxidizing agents, air.
RUO – Research Use Only
Maria J Climent et. al. Solid catalysts for multistep reactions: one-pot synthesis of 2,3-dihydro-1,5-benzothiazepines with solid acid and base catalysts. Chemsuschem Chemistry And Sustainability, Energy & Materials. 2014, 7(4), 1177-1185.
Valfredo Azevedo Lemos, , Patrícia Xavier Baliza. Amberlite XAD-2 functionalized with 2-aminothiophenol as a new sorbent for on-line preconcentration of cadmium and copper. Talanta. 2005, 67 (3), 564-570.
Reacts with carboxylic acid chlorides in N-methylpyrrolidinone to give 2-substituted benzothiazoles: Synth. Commun., 20, 3379 (1990), and with substituted benzonitriles in the presence of sodium hydride to give 2-arylbenzothiazoles: Heterocycles, 38, 1001 (1994).