| Weight | 123.155 g/mol |
|---|---|
| Formula | C7H9NO |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
2-Amino-5-methylphenol (2835-98-5)
6-amino-m-cresol
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- The inhibitive effect of 6-amino-m-cresol and its Schiff base on the corrosion of mild steel in 0.5 M HCI medium (Materials Chemistry and Physics, 2008)
- Synthesis, structural characterization and catalytic activity study of Mn(II), Fe(III), Ni(II), Cu(II) and Zn(II) complexes of quinoxaline-2-carboxalidine-2-amino-5-methylphenol: Crystal structure of the nickel(II) complex (Polyhedron, 2010)
- Synthesis, characterization, and structure of a new cobalt(II) Schiff-base complex with quinoxaline- 2-carboxalidine-2-amino-5-methylphenol (Journal of Coordination Chemistry, 2010)
- Antitumor activity of 2-amino-4,4 alpha-dihydro-4 alpha, 7-dimethyl-3H-phenoxazine-3-one, a novel phenoxazine derivative produced by the reaction of 2-amino-5-methylphenol with bovine hemolysate. (Anti-Cancer Drugs, 1996)
- Copper modified poly-6-amino-m-cresol (poly-AmC/Cu) coating for mild steel protection (Surface & Coatings Technology, 2009)
- Fabrication and in vitro degradation study of novel optically active polymers derived from amino acid containing diacids and 4,4'-thiobis(2-tert-butyl-5-methylphenol) (Journal of Polymer Research, 2011)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 6-amino-m-cresol
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SMILESCC1=CC(=C(C=C1)N)O
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InChIKeyHCPJEHJGFKWRFM-UHFFFAOYSA-N
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