| Weight | 154.125 g/mol |
|---|---|
| Formula | C6H6N2O3 |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
2-AMINO-5-NITROPHENOL (121-88-0)
3-hydroxy-4-aminonitrobenzene · Rodol YBA · Ursol Yellow Brown A
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- Amino acid and peptide analysis using derivatization with p-nitrophenol-2,5-dihydroxyphenylacetate bis-tetrahydropyranyl ether and capillary electrophoresis with electrochemical detection (Journal of Pharmaceutical and Biomedical Analysis, 2003)
- Process for preparing 2-amino-5-nitrophenol derivatives (1985)
- The structure of 2-amino-5-nitrophenol: a comparison with 2-aminophenol (Acta Crystallographica Section B Structural Crystallography and Crystal Chemistry, 1980)
- Peroxidase-Catalyzed Co-oxidation of 3,3,5,5-Tetramethylbenzidine with 2-Amino-4-nitrophenol, 4,4-Dihydroxydiphenylsulfone, and Their Polydisulfides in Aqueous and Micellar Media (Biochemistry, 2001)
- 2-Amino-4,4-dihydro-4,7-dimethyl-3H-phenoxazin-3-one as an unexpected product from reduction of 5-methyl-2-nitrophenol (Tetrahedron Letters, 2015)
- Use of 5-amino-2-nitrophenol derivatives in hair dyeing compositions, process for the preparation of these compounds, and 5-amino-2-nitrophenol derivatives (1987)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 3-hydroxy-4-aminonitrobenzene
- Rodol YBA
- Ursol Yellow Brown A
- 5-nitro-2-aminophenol
- 3-nitro-6-aminophenol
- 2-hydroxy-4-nitroaniline
-
SMILESC1=CC(=C(C=C1[N+](=O)[O-])O)N
-
InChIKeyDOPJTDJKZNWLRB-UHFFFAOYSA-N
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