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559318

Sigma-Aldrich

1-(2-Bromoethyl)naphthalene

97%

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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

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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

Signal Word

Warning

Hazard Statements

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

230.0 °F - closed cup

Flash Point(C)

110 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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’.

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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)
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)

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