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About This Item
Linear Formula:
C6H5CH(CH3)Br
CAS Number:
Molecular Weight:
185.06
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
209-560-2
MDL number:
Assay:
97%
Form:
liquid
Quality Level
assay
97%
form
liquid
refractive index
n20/D 1.56 (lit.)
bp
94 °C/16 mmHg (lit.)
density
1.356 g/mL at 25 °C (lit.)
functional group
bromo, phenyl
SMILES string
CC(Br)c1ccccc1
InChI
1S/C8H9Br/c1-7(9)8-5-3-2-4-6-8/h2-7H,1H3
InChI key
CRRUGYDDEMGVDY-UHFFFAOYSA-N
Application
(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
- as initiator in the synthesis of bromine terminated polyp-methoxystyrene and polystyrene via atom transfer radical polymerization
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
10 - Combustible liquids
wgk
WGK 3
flash_point_f
179.6 °F - closed cup
flash_point_c
82 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
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Design of effective systems for controlled radical polymerization of styrene: Application of 4, 49-dimethyl and 5, 59-dimethyl 2, 29-bipyridine copper (II) complexes.
Schubert US, et al.
Macromolecular Rapid Communications, 20, 351-355 (1999)
Synthesis of block copolymers by combination of atom transfer radical and promoted cationic polymerization mechanisms.
Baskan Duz A and Yagci Y.
Eur. Polymer J., 35(11), 2031-2038 (1999)
Simple preparation of chiral 1, 3-dimethyl-2-iminoimidazolidines (monocyclic guanidines) and applications to asymmetric alkylative esterification.
Isobe T, et al.
Tetrahedron Asymmetry, 9(10), 1729-1735 (1998)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 238104-25G | 04061838786630 |
| 238104-100G | 04061838786623 |
