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About This Item
Linear Formula:
ZnBr2
CAS Number:
Molecular Weight:
225.20
UNSPSC Code:
12352302
PubChem Substance ID:
EC Number:
231-718-4
MDL number:
InChI key
VNDYJBBGRKZCSX-UHFFFAOYSA-L
InChI
1S/2BrH.Zn/h2*1H;/q;;+2/p-2
SMILES string
Br[Zn]Br
grade
anhydrous
assay
99.999% trace metals basis
form
beads, crystalline
particle size
-10 mesh
mp
394 °C (lit.)
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Application
Anhydrous crystalline zinc bromide is used for the synthesis of ZnS based composite semiconductor photocatalyst. It is also widely studied to understand the structure-property relationships in zinc bromide and hence predict its different applications. Zinc bromide is a widely used catalyst for stereochemical reactions and is also an important brominating agent.
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Chronic 2 - Skin Corr. 1B - Skin Sens. 1
Storage Class
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Regulatory Information
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Chieh; C.; et al.
Zeitschrift fur Kristallographie, 166, 189-189 (1984)
Batsanov; S. S.; et al.
Journal of Molecular Structure, 980, 225-225 (2010)
Teiichi Murakami et al.
Carbohydrate research, 343(8), 1297-1308 (2008-04-15)
Reactions of O-benzoylated glucopyranosyl halide (I, Br), isolated or generated in situ from per-benzoylated glucose (8a) and trimethylsilyl halide, with various alcohols were efficiently promoted by zinc halide (Cl, Br) or N-bromosuccinimide with a catalytic ZnI(2) to give the corresponding
Toshiaki Sasada et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 17(34), 9385-9394 (2011-07-23)
The [5+1] annulation of enamidines, which were prepared from functionalized silanes, organolithium compounds and two nitriles, with N,N-dimethylformamide dialkyl acetals as the C1 unit is described, leading to the synthesis of tri- and tetrasubstituted pyrimidine derivatives under catalyst- and solvent-free
Isabelle Aillaud et al.
Molecules (Basel, Switzerland), 15(11), 8144-8155 (2010-11-13)
A methodological study devoted to the Mannich-like multicomponent synthesis of the antiplatelet agent (±)‑clopidogrel (7) and the ethyl ester analogue 6 is described. The process involves the formation of 2-chlorophenyl zinc bromide (2) and its subsequent reaction with an alkyl
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