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Merck
CN

760625

Zinc bromide

crystalline, anhydrous, beads, -10 mesh, 99.999% trace metals basis

Synonym(s):

Zinc dibromide

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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:
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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.

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Danger

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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