(1-Bromoethyl)benzene, 97%, Thermo Scientific Chemicals
(1-Bromoethyl)benzene, 97%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

(1-Bromoethyl)benzene, 97%, Thermo Scientific Chemicals

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100 g
25 g
500 g
Catalog number A16839.22
also known as A16839-22
Price (USD)/ Each
122.00
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Quantity:
100 g
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Price (USD)/ Each
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(1-Bromoethyl)benzene, 97%, Thermo Scientific Chemicals
Catalog numberA16839.22
Price (USD)/ Each
122.00
-
Add to cart
Chemical Identifiers
CAS585-71-7
IUPAC Name(1-bromoethyl)benzene
Molecular FormulaC8H9Br
InChI KeyCRRUGYDDEMGVDY-UHFFFAOYNA-N
SMILESCC(Br)C1=CC=CC=C1
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SpecificationsSpecification SheetSpecification Sheet
Assay (GC)≥96.0%
FormLiquid
Identification (FTIR)Conforms
Appearance (Color)Clear colorless to pale yellow to yellow to brown to gray
Refractive Index1.5585-1.5635 @ 20?C
(1-Bromoethyl)benzene has been employed in controlled radical polymerization of styrene, in asymmetric esterification of benzoic acid in the presence of a chiral cyclic guanidine and as initiator in the synthesis of bromine terminated polyp-methoxystyrene and polystyrene via atom transfer radical polymerization.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
(1-Bromoethyl)benzene has been employed in controlled radical polymerization of styrene, in asymmetric esterification of benzoic acid in the presence of a chiral cyclic guanidine and as initiator in the synthesis of bromine terminated polyp-methoxystyrene and polystyrene via atom transfer radical polymerization.

Solubility
Soluble in alcohol, ether, and benzene.

Notes
Moisture Sensitive. Do not store together with strongly basic and oxidizing materials.
RUO – Research Use Only

General References:

  1. F. Seutter-berlage; L. P. C. Delbressine; F. L. M. Smeets & M. A. P. Wagenaars-zegers. Mechanism of formation of mercapturic acids from (1-bromoethyl)benzene and (2-bromoethyl)benzene in the rat. Xenobiotica: the fate of foreign compounds in biological systems.2012, 105 (10), 397-398.