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154571

Sigma-Aldrich

1-Methoxynaphthalene

≥98%

Synonym(s):

Methyl 1-naphthyl ether, NSC 5530

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About This Item

Linear Formula:
C10H7OCH3
CAS Number:
2216-69-5
Molecular Weight:
158.20
Beilstein/REAXYS Number:
774884
EC Number:
218-696-1
MDL number:
MFCD00003924
UNSPSC Code:
12352100
PubChem Substance ID:
24849454
NACRES:
NA.22

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.

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

233.6 °F - closed cup

flash_point_c

112 °C - closed cup

ppe

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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