Skip to Content
Merck

Skip To

200174

Sigma-Aldrich

2-Bromo-6-methoxynaphthalene

97%

Synonym(s):

2-Bromo-6-methoxynaphthalene, 2-Methoxy-6-bromonaphthalene, 6-Bromo-2-methoxynaphthalene, 6-Methoxy-2-bromonaphthalene, 6-Methoxynaphth-2-yl bromide

Sign Into View Organizational & Contract Pricing

About This Item

Linear Formula:
BrC10H6OCH3
CAS Number:
Molecular Weight:
237.09
Beilstein:
2043874
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Pricing and availability is not currently available.
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

Quality Level

Assay

97%

mp

106-109 °C (lit.)

functional group

bromo

SMILES string

COc1ccc2cc(Br)ccc2c1

InChI

1S/C11H9BrO/c1-13-11-5-3-8-6-10(12)4-2-9(8)7-11/h2-7H,1H3

InChI key

AYFJBMBVXWNYLT-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

Application

2-Bromo-6-methoxynaphthalene was used in the synthesis of nabumetone [4-(6-methoxy-2-naphthalenyl)-2-butanone] by Heck reaction[1].

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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

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.

Already Own This Product?

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

Visit the Document Library

An efficient, one-pot, synthesis of dithiocarbamates from the corresponding alcohols using Mitsunobu's reagent.
Chaturvedi D and Ray S.
Tetrahedron Letters, 47(8), 1307-1309 (2006)
Copolymerization of ethylene sulfide and carbon disulfide.
Soga K, et al.
Journal of Polymer Science Part A: Polymer Chemistry, 14(3), 677-684 (1976)
Nanosized titania and zirconia as catalysts for hydrolysis of carbon disulfide.
Yue Y, et al.
Applied Catalysis. B, Environmental, 46(3), 561-572 (2003)
1, 3-Dithiolium carbenes from acetylenes and carbon disulfide.
Hartzler HD.
Journal of the American Chemical Society, 95(13), 4379-4387 (1973)
Xanthogenation of lignocarbohydrates by carbon disulfide.
Efanov MV and Pershina LA.
Chemistry of Natural Compounds, 38(1), 90-94 (2002)

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