154571
1-Methoxynaphthalene
≥98%
Synonym(s):
Methyl 1-naphthyl ether, NSC 5530
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About This Item
Linear Formula:
C10H7OCH3
CAS Number:
Molecular Weight:
158.20
Beilstein:
774884
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Quality Level
Assay
≥98%
form
liquid
refractive index
n20/D 1.621 (lit.)
bp
135-137 °C/12 mmHg (lit.)
density
1.09 g/mL at 25 °C (lit.)
SMILES string
COc1cccc2ccccc12
InChI
1S/C11H10O/c1-12-11-8-4-6-9-5-2-3-7-10(9)11/h2-8H,1H3
InChI key
NQMUGNMMFTYOHK-UHFFFAOYSA-N
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Application
1-Methoxynaphthalene was used to study the peroxygenase activity of CcP. It was also used to synthesize prenyl naphthalen-ols.
WGK
WGK 3
Flash Point(F)
233.6 °F
Flash Point(C)
112 °C
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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James E Erman et al.
BMC biochemistry, 14, 19-19 (2013-07-31)
The cytochrome P450s are monooxygenases that insert oxygen functionalities into a wide variety of organic substrates with high selectivity. There is interest in developing efficient catalysts based on the "peroxide shunt" pathway in the cytochrome P450s, which uses H2O2 in
Kazutoshi Shindo et al.
Bioscience, biotechnology, and biochemistry, 75(3), 505-510 (2011-03-11)
We performed combinational bioconversion of substituted naphthalenes with PhnA1A2A3A4 (an aromatic dihydroxylating dioxygenase from marine bacterium Cycloclasticus sp. strain A5) and prenyltransferase NphB (geranyltransferase from Streptomyces sp. strain CL190) or SCO7190 (dimethylallyltransferase from Streptomyces coelicolor A3(2)) to produce prenyl naphthalen-ols.
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