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498491

Sigma-Aldrich

4-Ethoxy-4-oxobutylzinc bromide solution

0.5 M in THF

Synonym(s):

(4-Ethoxy-4-oxobutyl)zinc(II) bromide, Bromo[4-ethoxy-4-(oxo-κO)butyl-κC]zinc

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About This Item

Linear Formula:
C2H5O2C(CH2)3ZnBr
CAS Number:
Molecular Weight:
260.44
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.22

Quality Level

concentration

0.5 M in THF

density

0.976 g/mL at 25 °C

storage temp.

2-8°C

SMILES string

CCOC(=O)CCC[Zn]Br

InChI

1S/C6H11O2.BrH.Zn/c1-3-5-6(7)8-4-2;;/h1,3-5H2,2H3;1H;/q;;+1/p-1

InChI key

QRIVZBPOANGBFR-UHFFFAOYSA-M

Related Categories

Application

4-Ethoxy-4-oxobutylzinc bromide can be used:
  • As an intermediate in one of the key synthetic steps for the preparation of acrylic acid derivatives as EP3 receptor antagonists.
  • As an intermediate in the final step of the total synthesis of a natural product mucosin.
  • As a substrate in the synthesis of multi-substituted haloalkenes by reacting with 1-haloalkenes via Negishi cross-coupling reaction.

Legal Information

Product of Rieke Metals, Inc.
Rieke is a registered trademark of Rieke Metals, Inc.

Pictograms

Health hazardExclamation mark

Signal Word

Warning

Hazard Statements

Precautionary Statements

Hazard Classifications

Carc. 2 - Eye Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Supplementary Hazards

WGK

WGK 3

Flash Point(F)

-6.2 °F

Flash Point(C)

-21.2 °C

Regulatory Information

危险化学品

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Synthesis of the multisubstituted halogenated olefins via cross-coupling of dihaloalkenes with alkylzinc bromides
Andrei D and Wnuk SF
The Journal of Organic Chemistry, 71(1), 405-408 (2006)
Total Synthesis of (-)-Mucosin and Revision of Structure
Nolsoe JMJ, et al.
The Journal of Organic Chemistry, 83(24), 15066-15076 (2018)
Discovery of a series of acrylic acids and their derivatives as chemical leads for selective EP3 receptor antagonists
Asada M, et al.
Bioorganic & Medicinal Chemistry, 17(18), 6567-6582 (2009)
Stereopermutation on the Putative Structure of the Marine Natural Product Mucosin
Antonsen SG, et al.
Molecules (Basel), 22(10), 1720-1720 (2017)

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