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451398

Sigma-Aldrich

Zinc bromide

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

동의어(들):

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 코드:
12352302
eCl@ss:
38150410
PubChem Substance ID:
24868627
NACRES:
NA.23

제품 라인

AnhydroBeads™

Quality Level

100

분석

99.999% trace metals basis

반응 적합성

reagent type: catalyst
core: zinc

불순물

≤15.0 ppm Trace Metal Analysis

입자 크기

−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

유사한 제품을 찾으십니까? 방문 제품 비교 안내

애플리케이션

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

법적 정보

AnhydroBeads is a trademark of Sigma-Aldrich Co. LLC

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

8B - Non-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

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시험 성적서(COA)

Lot/Batch Number
0000212218
0000183169
MKCD0309
MKCB3621
MKBV9952V

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Zinc chloride anhydrous, free-flowing, Redi-Dri™, reagent grade, ≥98%

Sigma-Aldrich

793523

Zinc chloride

Lead(II) bromide 99.999% trace metals basis

Sigma-Aldrich

398853

Lead(II) bromide

Zinc chloride reagent grade, ≥98%

Sigma-Aldrich

208086

Zinc chloride

Zinc chloride 99.999% trace metals basis

Sigma-Aldrich

229997

Zinc chloride

Franz, A.K. Woerpel, K.A.
Journal of the American Chemical Society, 121, 949-949 (1999)
J R Baker et al.
Organic letters, 9(1), 45-48 (2006-12-29)
[reaction: see text] A key structural feature of the Neocarzinostatin chromophore is a reactive epoxydiyne. We present here a new method for the preparation of epoxydiynes by the addition of an allenyl zinc bromide to a propargylic ketone.
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.
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