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2-Ethylnaphthalene exhibits inhibitory activity against CYP1A2, CYP2A5, and CYP2A6 and can be used in biochemical experiments and drug synthesis.
Description | 2-Ethylnaphthalene exhibits inhibitory activity against CYP1A2, CYP2A5, and CYP2A6 and can be used in biochemical experiments and drug synthesis. |
In vitro | Using 2-Ethylnaphthalene as a model substrate, the oxidation can be carried out in conventional biphasic or monophasic solvent systems. In either case, the reaction rate and product selectivity are identical. The reaction products indicate that the aromatic ring system is oxidized preferentially over the alkyl chain. [1] |
Molecular Weight | 156.22 |
Formula | C12H12 |
Cas No. | 939-27-5 |
Smiles | C=1C=CC=2C=C(C=CC2C1)CC |
Storage | store at 4°C | Shipping with blue ice/Shipping at ambient temperature. |
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