Weight | 200.237 g/mol |
---|---|
Formula | C13H12O2 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 1 |
Aromatic Rings | 2 |
Rotatable Bonds | 3 |
3-Phenoxybenzyl alcohol (13826-35-2)
3-phenoxybenzylalcohol
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- The pyrethroid metabolites 3-phenoxybenzoic acid and 3-phenoxybenzyl alcohol do not exhibit estrogenic activity in the MCF-7 human breast carcinoma cell line or SpragueDawley rats (Toxicology, 2010)
- Chiral-phase high-performance liquid chromatographic separation of enantiomers of pyrethroid insecticide esters derived from -cyano-3-phenoxybenzyl alcohol (Journal of Chromatography A, 1983)
- Chemo-enzymatic synthesis of (S)--cyano-3-phenoxybenzyl alcohol (Tetrahedron-asymmetry, 1998)
- Permethrin absorption not detected in single-pass perfused rabbit ear, and absorption with oxidation of 3-phenoxybenzyl alcohol. (Archives of Toxicology, 1997)
- The kinetic study on lipase-catalyzed transesterification of -cyano-3-phenoxybenzyl alcohol in organic media (Journal of Molecular Catalysis B-enzymatic, 2002)
- The metabolism of 3phenoxybenzyl alcohol, a pyrethroid metabolite, in plants (Pesticide Science, 1981)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 3-phenoxybenzylalcohol
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SMILESC1=CC=C(C=C1)OC2=CC=CC(=C2)CO
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InChIKeyKGANAERDZBAECK-UHFFFAOYSA-N
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Synthesis
Reactant
+
phenoxyalcohol
(Dakin oxidation)
Similar Compounds
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Norfenefrine
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3-propoxybenzoic acid
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