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193065-68-8

193065-68-8 Structure

193065-68-8 Structure
IdentificationBack Directory
[Name]

3-ETHOXY-3-OXOPROPYLZINC BROMIDE
[CAS]

193065-68-8
[Synonyms]

zinc bromide soL
3-Ethoxy-3-oxopropyL
3-ETHOXY-3-OXOPROPYLZINC BROMIDE
2-(Ethoxycarbonyl)ethylzinc bromide
(3-ethoxy-3-oxopropyl)zinc(II) broMide
3-ethoxy-3-oxopropylzinc bromide solution
2-(Ethoxycarbonyl)ethylzinc bromide, 0.5M in THF
3-Ethoxy-3-oxopropylzinc bromide solution 0.5 in THF
3-Ethoxy-3-oxopropylzinc broMide solution 0.5 M in THF
3-ETHOXY-3-OXOPROPYLZINC BROMIDE, 0.5MSO LUTION IN TETRAHYDROFURAN
[Molecular Formula]

C5H9BrO2Zn
[MDL Number]

MFCD00671976
[MOL File]

193065-68-8.mol
[Molecular Weight]

246.42
Chemical PropertiesBack Directory
[density ]

0.972 g/mL at 25 °C
[Fp ]

1 °F
[storage temp. ]

2-8°C
[Water Solubility ]

Reacts with water.
[Exposure limits]

ACGIH: TWA 50 ppm; STEL 100 ppm (Skin)
OSHA: TWA 200 ppm(590 mg/m3)
NIOSH: IDLH 2000 ppm; TWA 200 ppm(590 mg/m3); STEL 250 ppm(735 mg/m3)
[InChI]

1S/C5H9O2.BrH.Zn/c1-3-5(6)7-4-2;;/h1,3-4H2,2H3;1H;/q;;+1/p-1
[InChIKey]

XLKAROLEWCMBDC-UHFFFAOYSA-M
[SMILES]

CCOC(=O)CC[Zn]Br
Safety DataBack Directory
[Symbol(GHS) ]

GHS hazard pictogramsGHS hazard pictogramsGHS hazard pictogramsGHS hazard pictograms
GHS02,GHS05,GHS07,GHS08
[Signal word ]

Danger
[Hazard statements ]

H261-H318-H333-H225-H302-H314-H335-H351
[Precautionary statements ]

P210-P260-P280-P305+P351+P338-P370+P378-P403+P235-P223-P303+P361+P353-P405-P501a
[Hazard Codes ]

F,Xi,Xn
[Risk Statements ]

11-19-36/37-40
[Safety Statements ]

16-26-29-33-36/37
[RIDADR ]

UN 3399 4.3/PG 2
[WGK Germany ]

1
[HazardClass ]

4.3
[PackingGroup ]

II
[HS Code ]

29319090
[Storage Class]

3 - Flammable liquids
[Hazard Classifications]

Acute Tox. 4 Oral
Carc. 2
Flam. Liq. 2
Skin Corr. 1B
STOT SE 3
Hazard InformationBack Directory
[Uses]

3-Ethoxy-3-oxopropylzinc bromide is a reagent used to insert ethyl propanoate group to the substrate. It can be used in:
  • Synthesis of γ-keto esters from aryl chlorides.
  • Synthesis of sulfones from 1,4-diazabicyclo[2.2.2]octane bis(sulfur dioxide) (DABSO) and alkyl halides.
  • Negishi cross-couplings with aryl vinyl phosphates to synthesize 1,1-disubstituted alkenes.

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