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451398

Sigma-Aldrich

Zinc bromide

AnhydroBeads™, −10 mesh, 99.999% trace metals basis

Synonym(s):

Zinc dibromide

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About This Item

Linear Formula:
ZnBr2
CAS Number:
7699-45-8
Molecular Weight:
225.20
EC Number:
231-718-4
MDL number:
MFCD00011294
UNSPSC Code:
12352302
eCl@ss:
38150410
PubChem Substance ID:
24868627
NACRES:
NA.23
assay:
99.999% trace metals basis
grade:
synthesis grade
solubility:
diethyl ether: slightly soluble(lit.)
ethanol: very soluble(lit.)

grade

synthesis grade

product line

AnhydroBeads™

assay

99.999% trace metals basis

reaction suitability

reagent type: catalyst
core: zinc

impurities

≤15.0 ppm Trace Metal Analysis

particle size

−10 mesh

bp

~670 °C/1 atm (lit.)

mp

394 °C (lit.)

solubility

diethyl ether: slightly soluble(lit.)
ethanol: very soluble(lit.)

SMILES string

Br[Zn]Br

InChI

1S/2BrH.Zn/h2*1H;/q;;+2/p-2

InChI key

VNDYJBBGRKZCSX-UHFFFAOYSA-L

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Application

Optimal catalyst for stereospecific and regioselective reaction of silacyclopropanes with carbonyl compounds.

Legal Information

AnhydroBeads is a trademark of Sigma-Aldrich Co. LLC

accessory

Product No.
Description
Pricing

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Danger

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 2 - Eye Dam. 1 - Skin Corr. 1B - Skin Sens. 1

Storage Class

8B - Non-combustible corrosive hazardous materials

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

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Certificates of Analysis (COA)

Lot/Batch Number
0000212218
0000183169
MKCD0309
MKCB3621
MKBV9952V

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Yasuhiro Inui et al.
Chemical & pharmaceutical bulletin, 57(10), 1158-1160 (2009-10-06)
Asymmetric intermolecular hydroacylation between salicylaldehyde (1) and 1,5-hexadiene (2) using a combination of [RhCl(C(8)H(14))(2)](2) (0.10 eq), (S)-BINAP (0.10 eq), and ZnBr(2) (0.20 eq) afforded an enantiomerically enriched hydroacylated product iso-3 of 84% ee, along with an achiral product normal-3.
Fernando Ferreira et al.
Nucleosides, nucleotides & nucleic acids, 24(5-7), 1009-1013 (2005-10-27)
An oligonucleotide protected with N-(trimethylsilyloxycarbonyl) (Teoc) and P-(trimethylsilylethanol) (Tse) groups was synthesized and deprotected by a single ZnBr2 treatment. Finally it was released from the solid support by cleavage of a disulfide linkage with TCEP. The olgonucleotide was obtained without
Biswajit Kalita et al.
Chemical communications (Cambridge, England), (36)(36), 4291-4293 (2008-09-20)
Benzylic and allylic hydrocarbons are selectively converted to the corresponding sulfonamides by a ZnBr2-H2O-catalyzed reaction with PhI=NTs; saturated adamantane is aminosulfonated at the tertiary C-H bond.
Thomas Hameury et al.
Organic letters, 11(11), 2397-2400 (2009-05-09)
A diastereodivergent addition of allenylzincs to aryl glyoxylates was observed depending on the method used for the preparation of the allenylzinc reagent. The allenylzincs were prepared from propargylic benzoates in the presence of a palladium catalyst or by metalation of
Yang Yu et al.
Preparative biochemistry & biotechnology, 37(4), 381-387 (2007-09-13)
Zinc bromide catalyzes the three component condensation reaction of an aldehyde, urea, and beta-ketoester or beta-diketone under solvent-free conditions to afford the corresponding dihydropyrimidinones (DHPMs) with moderate to high yields in short reaction time. The present method is very effective
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