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Merck
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문서

230022

Sigma-Aldrich

Zinc bromide

99.999% trace metals basis

동의어(들):

Zinc dibromide

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모든 사진(1)

About This Item

Linear Formula:
ZnBr2
CAS Number:
7699-45-8
Molecular Weight:
225.20
EC Number:
231-718-4
MDL number:
MFCD00011294
UNSPSC 코드:
12352302
eCl@ss:
38150410
PubChem Substance ID:
24853770
NACRES:
NA.23

분석

99.999% trace metals basis

형태

powder and chunks

반응 적합성

reagent type: catalyst
core: zinc

불순물

≤15.0 ppm Trace Metal Analysis

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

유사한 제품을 찾으십니까? 방문 제품 비교 안내

애플리케이션

Zinc bromide supported on silica or montmorillonite can be used as a selective catalyst for the bromination of aromatic substrates.

It can be used as starting material to prepare poly(ethylene oxide)/ zinc salt systems, which can be used as polymer electrolytes.

Itcan also be used to prepare ZnO nanoparticles.

픽토그램

CorrosionExclamation markEnvironment
GHS05,GHS07,GHS09

신호어

Danger

유해 및 위험 성명서

H302,H314,H317,H411

Hazard Classifications

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

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

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

시험 성적서(COA)

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문서 라이브러리 방문

이미 열람한 고객

Slide 1 of 3

1 of 3

Zinc chloride anhydrous, free-flowing, Redi-Dri™, ACS reagent, ≥97%

Sigma-Aldrich

746355

Zinc chloride

Magnesium bromide 98%

Sigma-Aldrich

360074

Magnesium bromide

Lead(II) bromide 99.999% trace metals basis

Sigma-Aldrich

398853

Lead(II) bromide

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
Direct synthesis of alkynylstannanes: ZnBr2 catalyst for the reaction of tributyltin methoxide and terminal alkynes.
Kensuke Kiyokawa et al.
Angewandte Chemie (International ed. in English), 50(44), 10393-10396 (2011-09-15)
Frederic G Buono et al.
Organic letters, 10(23), 5325-5328 (2008-11-05)
Kinetic studies using reaction calorimetry were conducted under synthetically relevant conditions to study the effect of additives in the cyanation of bromobenzene catalyzed by palladium complexes. This work demonstrates that the addition of a catalytic amount of ZnBr(2) facilitates the
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
Franz, A.K. Woerpel, K.A.
Journal of the American Chemical Society, 121, 949-949 (1999)
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