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Merck
CN

406023

Diethylzinc solution

1.0 M in heptane

Synonym(s):

Zincdiethyl

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About This Item

Linear Formula:
(C2H5)2Zn
CAS Number:
557-20-0
Molecular Weight:
123.51
UNSPSC Code:
12352103
NACRES:
NA.22
PubChem Substance ID:
24865350
MDL number:
MFCD00009021
Beilstein/REAXYS Number:
3587207

Key Documents

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InChI

1S/2C2H5.Zn/c2*1-2;/h2*1H2,2H3;

SMILES string

CC[Zn]CC

InChI key

HQWPLXHWEZZGKY-UHFFFAOYSA-N

form

liquid

concentration

1.0 M in heptane

bp

98 °C

density

0.74 g/mL at 25 °C

Quality Level

100

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Application

Diethylzinc solution can be used in the synthesis of:
  • Bis(pyridylpyrrolyl)zinc luminescent complexes.
  • A versatile building block, 5-(ketoaryl)thiazole.
  • ZnxCd1-xSe nanocrystals having high luminescence properties.

signalword

Danger

target_organs

Central nervous system

supp_hazards

EUH014

Storage Class

4.2 - Pyrophoric and self-heating hazardous materials

wgk

WGK 3

flash_point_f

12.2 °F - closed cup

flash_point_c

-11 °C - closed cup

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - Asp. Tox. 1 - Eye Dam. 1 - Flam. Liq. 2 - Pyr. Liq. 1 - Skin Corr. 1B - STOT SE 3 - Water-react. 1

Regulatory Information

危险化学品
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Certificates of Analysis (COA)

Lot/Batch Number
SHBS7875
SHBS7874
SHBS5978
SHBR7171
SHBR7170

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Composition-Tunable ZnxCd1-xSe nanocrystals with high luminescence and stability.
Xinhua Z, et al.
Journal of the American Chemical Society, 125(28), 8589-8594 (2003)
Pyridylpyrrolides as alternatives to cyclometalated phenylpyridine ligands: synthesis and characterization of luminescent zinc and boron pyridylpyrrolide complexes.
Klappa JJ, et al.
Dalton Transactions, 883-891 (2004)
Practical synthesis of a highly functionalized thiazole ketone.
Frey LF, et al.
Tetrahedron, 59(33), 6363-6373 (2003)
Tummanapalli Satyanarayana et al.
Organic letters, 9(2), 251-253 (2007-01-16)
A strong asymmetric amplification is observed in the addition of diethylzinc on aromatic aldehydes in the presence of the bistriflamide of trans-1,2-diaminocyclohexane 3a. The asymmetric amplification originates from the insolubility of the catalyst precursor 3a of low enantiomeric excess (ee)
Efficient chirality switching in the addition of diethylzinc to aldehydes in the presence of simple chiral alpha-amino amides.
M Isabel Burguete et al.
Angewandte Chemie (International ed. in English), 46(47), 9002-9005 (2007-09-26)
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