| Weight | 123.155 g/mol |
|---|---|
| Formula | C7H9NO |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
4-Aminobenzyl alcohol (623-04-1)
p-aminobenzyl alcohol
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- Schiff bases derived from p-aminobenzyl alcohol as trigger groups for pH-dependent prodrug activation (Tetrahedron Letters, 2010)
- Water-soluble conducting copolymers of o-aminobenzyl alcohol and diphenylamine-4-sulfonic acid (Macromolecules, 1994)
- Metabolites of p-aminobenzoic acid III. A metabolic pathway of p-aminobenzoic acid resulting in the sequential formation of p-aminobenzyl alcohol and p-hydroxyaniline (Biochimica et Biophysica Acta, 1963)
- Studies on 1,3-benzoxazines. VI. Formation of quinazolines and 4H-3,1-benzoxazines by the reaction of 4-chloro-2H-1,3-benzoxazines with aminoacetophenone, aminobenzophenone and aminobenzyl alcohol derivatives. (Chemical & Pharmaceutical Bulletin, 1982)
- Process for producing 4-aminobenzyl alcohol derivatives (1965)
- Metablites of p-aminobenzoic acid V. Isolation and properties of p-aminobenzyl alcohol dehydrogenase (Biochimica et Biophysica Acta, 1973)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - p-aminobenzyl alcohol
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SMILESC1=CC(=CC=C1CO)N
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InChIKeyAXKGIPZJYUNAIW-UHFFFAOYSA-N
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