CAS 6274-29-9
:2-Amino-5-methoxythiophenol
- 2-Amino-5-methoxybenzenethiol
- 2-Mercapto-4-methoxyaniline
- Benzenethiol, 2-amino-5-methoxy-
- 5-Methoxy-2-aminothiophenol
- 2-Amino-5-methoxythiophenol
2-Amino-5-methoxybenzenethiol
CAS:Formula:C7H9NOSPurity:95%Color and Shape:SolidMolecular weight:155.21752-Amino-5-methoxybenzenethiol
CAS:2-Amino-5-methoxybenzenethiolFormula:C7H9NOSPurity:95%Color and Shape: green solidMolecular weight:155.22g/mol2-Amino-5-methoxybenzenethiol
CAS:Formula:C7H9NOSPurity:>98.0%(T)(HPLC)Color and Shape:Colorless to Yellow to Yellow green powder to crystalMolecular weight:155.222-Amino-5-methoxythiophenol (>90%)
CAS:Controlled ProductStability Unstable in Solution, Unstable in Air
Applications 2-Amino-5-methoxythiophenol is a chemical reagent used in the synthesis of antibacterial benzothiazepines.
References Bhasker, N. et al.: Elixir. Int. J., Dec, 29307 (2014); Pant, S. et al.: Int. J. Chem., 3, 360 (2014);Formula:C7H9NOSPurity:>90%Color and Shape:NeatMolecular weight:155.222-Amino-5-methoxythiophenol
CAS:2-Amino-5-methoxythiophenol is an organic compound that is used as a fluorescent probe for the measurement of mitochondrial membrane potential. The optimal reaction conditions are 3:1 methanol to water, with a reaction time of 10 minutes at room temperature. The demethylation of 2-amino-5-methoxythiophenol yields 3-mercaptopropionic acid, which can be used as a synthetic intermediate in other organic synthesis reactions. It has been found that the ring opening of 2-amino-5-methoxythiophenol occurs through oxidation and the formation of radicals. This reaction mechanism is supported by the photophysical properties observed in its fluorescence spectrum.
Formula:C7H9NOSPurity:Min. 95%Molecular weight:155.22 g/mol





