| Weight | 166.22 g/mol |
|---|---|
| Formula | C10H14O2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 3 |
Rhododendrol (501-96-2)
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- The Heck Reaction of Allylic Alcohols Catalyzed by Palladium Nanoparticles in Water: Chemoenzymatic Synthesis of (R)()Rhododendrol (Chemcatchem, 2011)
- Rhododendrol, a depigmentationinducing phenolic compound, exerts melanocyte cytotoxicity via a tyrosinasedependent mechanism (Pigment Cell & Melanoma Research, 2014)
- Tyrosinasecatalyzed oxidation of rhododendrol produces 2methylchromane6,7dione, the putative ultimate toxic metabolite: implications for melanocyte toxicity (Pigment Cell & Melanoma Research, 2014)
- Studies on the Constituents of Aceraceae Plants. IV. Carbon-13 Nuclear Magnetic Resonance Spectra of Acerogenin A, Rhododendrol and Related Compounds, and Structure of Aceroside IV from Acer nikoense (Chemical & Pharmaceutical Bulletin, 1983)
- Rhododendrol glycosides and phenyl glucoside esters from inner bark of Betula pubescens (Phytochemistry, 1994)
- Depigmentation caused by application of the active brightening material, rhododendrol, is related to tyrosinase activity at a certain threshold. (Journal of Dermatological Science, 2014)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC(CCC1=CC=C(C=C1)O)O
-
InChIKeySFUCGABQOMYVJW-UHFFFAOYSA-N
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