| Weight | 124.139 g/mol |
|---|---|
| Formula | C7H8O2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
salicyl alcohol (90-01-7)
saligenin · 2-methylol phenol · salicyl alcohol, monosodium salt
Score:
#1998 in Biochemistry
,
#5300 in Chemistry
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- Coordination and supramolecular aspects of the metal complexes of chiral N-salicyl--amino alcohol Schiff base ligands: Towards understanding the roles of weak interactions in their catalytic reactions (Coordination Chemistry Reviews, 2013)
- Saligenin analogs of sympathomimetic catecholamines. (Journal of Medicinal Chemistry, 1970)
- Neuropathological effects of phenyl saligenin phosphate in chickens (Neurotoxicology, 1987)
- Glucosylation of salicyl alcohol in cultured plant cells (Phytochemistry, 1983)
- Reaction of cresyl saligenin phosphate, the organophosphorus agent implicated in aerotoxic syndrome, with human cholinesterases: mechanistic studies employing kinetics, mass spectrometry, and X-ray structure analysis. (Chemical Research in Toxicology, 2011)
- Pathways of salicyl alcohol and salicin formation in Salix purpurea L. (Phytochemistry, 1967)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - saligenin
- 2-methylol phenol
- salicyl alcohol, monosodium salt
- 2-monomethylolphenol
- salicyl alcohol, disodium salt
- o-hydroxybenzyl alcohol
- salicyl alcohol, (ar)-isomer
-
SMILESC1=CC=C(C(=C1)CO)O
-
InChIKeyCQRYARSYNCAZFO-UHFFFAOYSA-N
- Pubchem - salicyl alcohol
- Wikipedia - salicyl alcohol
Salicyl alcohol (saligenin) is precursor of salicylic acid and is formed from salicin by enzymatic hydrolysis by Salicyl-alcohol beta-D-glucosyltransferase or by acid hydrolysis.
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salicyl alcohol
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