| Weight | 123.155 g/mol |
|---|---|
| Formula | C7H9NO |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
2-Aminobenzyl alcohol (5344-90-1)
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- Ruthenium-Catalyzed Oxidative Coupling and Cyclization Between 2-Aminobenzyl Alcohol and Secondary Alcohols Leading to Quinolines. (Tetrahedron, 2003)
- Multifunctional Catalysis of a Ruthenium-Grafted Hydrotalcite: One-Pot Synthesis of Quinolines from 2-Aminobenzyl Alcohol and Various Carbonyl Compounds via Aerobic Oxidation and Aldol Reaction. (Tetrahedron Letters, 2004)
- Synthesis, Structural Characterization, Redox and Antimicrobial Studies of Schiff Base Copper(II), Nickel(II), Cobalt(II), Manganese(ii), Zinc(II) and Oxovanadium(ii) Complexes derived from benzil and 2-Aminobenzyl Alcohol (Polish Journal of Chemistry, 2002)
- FT-Raman and FTIR spectra, assignments and ab initio calculations of 2-aminobenzyl alcohol (Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 2005)
- A rhodium-catalyzed route for oxidative coupling and cyclization of 2-aminobenzyl alcohol with ketones leading to quinolines (Journal of Heterocyclic Chemistry, 2005)
- Ruthenium-catalysed oxidative cyclisation of 2-aminobenzyl alcohol with ketones: modified Friedlaender quinoline synthesis (Chemical Communications, 2001)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC=C(C(=C1)CO)N
-
InChIKeyVYFOAVADNIHPTR-UHFFFAOYSA-N
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