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2-Ethylnaphthalene exhibits inhibitory activity against CYP1A2, CYP2A5, and CYP2A6 and can be used in biochemical experiments and drug synthesis.

| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 50 mg | $35 | - | In Stock | |
| 100 mg | $50 | - | In Stock |
| 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 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. |
Dissolve 2 mg of the compound in 100 μL DMSO
to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.
1) Add 100 μL of the DMSO
stock solution to 400 μL PEG300
and mix thoroughly until the solution becomes clear.
2) Add 50 μL Tween 80 and mix well until fully clarified.
3) Add 450 μL Saline,PBS or ddH2O
and mix thoroughly until a homogeneous solution is obtained.
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