CAS 1687-53-2
:5-Amino-2-methoxyphenol
- (3-Hydroxy-4-methoxyphenyl)amine
- 1687-53-2
- 2-Methoxy-5-aminophenol
- 3-Amino-6-methoxyphenol
- 3-Hydroxy-4-methoxyaniline
- 5-Amino-2-(methyloxy)phenol
- 5-Aminoguaiacol
- Guaiacol, 5-amino-
- Phenol, 5-amino-2-methoxy-
- 5-Amino-2-methoxyphenol
5-Amino-2-methoxyphenol, 98%
CAS:This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Sci
Formula:C7H9NO2Purity:98%Color and Shape:Brown to dark brown, PowderMolecular weight:139.15Phenol, 5-amino-2-methoxy-
CAS:Formula:C7H9NO2Purity:97%Color and Shape:SolidMolecular weight:139.15195-Amino-2-methoxyphenol
CAS:5-Amino-2-methoxyphenolFormula:C7H9NO2Purity:98%Color and Shape: brown solidMolecular weight:139.15g/mol3-Hydroxy-4-methoxyaniline
CAS:Formula:C7H9NO2Purity:>98.0%(GC)(T)Color and Shape:Light yellow to Amber to Dark green powder to crystalMolecular weight:139.155-Amino-2-methoxyphenol
CAS:Formula:C7H9NO2Purity:95%Color and Shape:Solid, Yellow to deep yellow red powderMolecular weight:139.1545-Amino-2-methoxyphenol
CAS:5-Amino-2-methoxyphenol is a p-hydroxybenzoic acid, which is an amide derivative of 5-amino-2-methoxybenzoic acid. It can be used to prepare a sample for the detection of fatty acids in human serum by cycle analysis. 5-Amino-2-methoxyphenol has been shown to have antinociceptive properties and can be used as a chemical precursor in the synthesis of other compounds. The reaction mechanism for 5-Amino-2-methoxyphenol has been determined using NMR spectroscopy and chemical structures. The compound is stable at neutral pH and reacts with hydrogen to form an intramolecular hydrogen bond between the hydroxyl group and the nitrogen atom on the amino group.
Formula:C7H9NO2Purity:Min. 95%Color and Shape:Brown PowderMolecular weight:139.15 g/mol





