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1-Methoxynaphthalene, 98+%, Thermo Scientific Chemicals
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Catalog number B24825.22
also known as B24825-22
Price (USD)/ Each
168.00
-
Quantity:
100 g
Price (USD)/ Each
168.00
1-Methoxynaphthalene, 98+%, Thermo Scientific Chemicals
Catalog numberB24825.22
Price (USD)/ Each
168.00
-
Chemical Identifiers
CAS2216-69-5
IUPAC Name1-methoxynaphthalene
Molecular FormulaC11H10O
InChI KeyNQMUGNMMFTYOHK-UHFFFAOYSA-N
SMILESCOC1=C2C=CC=CC2=CC=C1
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Specifications
Specification Sheet
Specification SheetAppearance (Color)Clear colorless to yellow to brown
Assay (GC)≥98.0%
FormLiquid
Refractive Index1.6190-1.6235 @ 20?C
1-Methoxynaphthalene is used in the study of peroxygenase activity of cytochrome c peroxidase. It is used as a precursor to synthesize prenyl naphthalene-ols, which shows antioxidative activity.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
1-Methoxynaphthalene is used in the study of peroxygenase activity of cytochrome c peroxidase. It is used as a precursor to synthesize prenyl naphthalene-ols, which shows antioxidative activity.
Solubility
Immiscible with water. Miscible with ether, carbon disulfide and benzene.
Notes
Keep container tightly closed in a dry and well-ventilated place. Incompatible with strong oxidizing agents.
1-Methoxynaphthalene is used in the study of peroxygenase activity of cytochrome c peroxidase. It is used as a precursor to synthesize prenyl naphthalene-ols, which shows antioxidative activity.
Solubility
Immiscible with water. Miscible with ether, carbon disulfide and benzene.
Notes
Keep container tightly closed in a dry and well-ventilated place. Incompatible with strong oxidizing agents.
RUO – Research Use Only
General References:
- Onoda, H.; Shoji, O.; Watanabe, Y. Acetate anion-triggered peroxygenation of non-native substrates by wild-type cytochrome P450s. Dalton Trans. 2015, 44 (34), 15316-15323.
- Govindarajan, M.; Ganasan, K.; Periandy, S.; Karabacak, M. Experimental (FT-IR and FT-Raman), electronic structure and DFT studies on 1-methoxynaphthalene. Spectrochim. Acta, Part A 2011, 79 (3), 646-653.