Skip to Content
MilliporeSigma
All Photos(1)

Key Documents

559318

Sigma-Aldrich

1-(2-Bromoethyl)naphthalene

97%

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C12H11Br
CAS Number:
Molecular Weight:
235.12
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

assay

97%

refractive index

n20/D 1.638 (lit.)

bp

237-238 °C/760 mmHg (lit.)

density

1.646 g/mL at 25 °C (lit.)

SMILES string

BrCCc1cccc2ccccc12

InChI

1S/C12H11Br/c13-9-8-11-6-3-5-10-4-1-2-7-12(10)11/h1-7H,8-9H2

InChI key

GPHCPUFIWQJZOI-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

General description

1-(2-Bromoethyl)naphthalene can be obtained from the reaction between 1-(2-hydroxyethyl)naphthalene and phosphorus tribromide.

Application

1-(2-Bromoethyl)naphthalene may be used to synthesize 2-iodo-1-[2-(1-naphthyl)ethyl]-1H-benzimidazole.

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

230.0 °F - closed cup

flash_point_c

110 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

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

Visit the Document Library

Potentially carcinogenic cyclopenta [a] phenanthrenes. Part IV. Synthesis of 17-ketones by the Stobbe condensation.
Coombs MM, et al.
J. Chem. Soc. Sect. C, 9, 1266-1271 (1970)
Access to aromatic ring-fused benzimidazoles using photochemical substitutions of the benzimidazol-2-yl radical.
O'Connell JM, et al.
Synthesis, 44(12), 3371-3377 (2012)

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