| Weight | 214.22 g/mol |
|---|---|
| Formula | C13H10O3 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 2 |
Phenyl salicylate (118-55-8)
salol
Score:
#42 in Physical chemistry
,
#1323 in Physics
,
#3837 in Chemistry
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- SPECIFIC-HEAT SPECTROSCOPY AND DIELECTRIC SUSCEPTIBILITY MEASUREMENTS OF SALOL AT THE GLASS TRANSITION (Physical Review B, 1990)
- Light-scattering investigation of and relaxation near the liquid-glass transition of the molecular glass Salol (Physical Review A, 1992)
- Neuroprotection by sodium salicylate against 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine-induced neurotoxicity (Brain Research, 2000)
- Non-steroidal anti-inflammatory drug sodium salicylate, but not diclofenac or celecoxib, protects against 1-methyl-4-phenyl pyridinium-induced dopaminergic neurotoxicity in rats (Brain Research, 2003)
- Light-scattering spectroscopy of the liquid-glass transition in CaKNO3 and in the molecular glass salol : extended-mode-coupling-theory analysis (Physical Review E, 1993)
- Fragility under pressure: Diamond anvil cell viscometry of ortho-terphenyl and salol (Journal of Chemical Physics, 1998)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - salol
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SMILESC1=CC=C(C=C1)OC(=O)C2=CC=CC=C2O
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InChIKeyZQBAKBUEJOMQEX-UHFFFAOYSA-N
- Pubchem - Phenyl salicylate
- Wikipedia - phenyl salicylate
Phenyl salicylate, or salol, is a chemical substance, introduced in 1886 by Marceli Nencki of Basel. It is synthesized by heating salicylic acid with phenol. Once used in sunscreens, phenyl salicylate is now used in the manufacture of some polymers, lacquers, adhesives, waxes, and polishes.
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Phenyl salicylate
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