Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

154571

Sigma-Aldrich

1-Methoxynaphthalene

≥98%

Synonym(s):

Methyl 1-naphthyl ether, NSC 5530

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

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

Quality Level

200

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

Looking for similar products? Visit Product Comparison Guide

Application

1-Methoxynaphthalene was used to study the peroxygenase activity of CcP. It was also used to synthesize prenyl naphthalen-ols.

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

233.6 °F - closed cup

Flash Point(C)

112 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
BCCD7137
BCBH0203V
1451817V
1451817
1411221

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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.

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service