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220809

Sigma-Aldrich

二乙基锌 溶液

15 wt. % in toluene

别名:

Zincdiethyl

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About This Item

线性分子式:
(C2H5)2Zn
CAS号:
557-20-0
分子量:
123.51
Beilstein:
3587207
MDL號碼:
MFCD00009021
分類程式碼代碼:
12352103
PubChem物質ID:
24853193
NACRES:
NA.22

形狀

liquid

品質等級

100

濃度

15 wt. % in toluene

密度

0.915 g/mL at 25 °C

SMILES 字串

CC[Zn]CC

InChI

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

InChI 密鑰

HQWPLXHWEZZGKY-UHFFFAOYSA-N

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應用

与 CF3I 共同用于 Rh(I) 催化的由 α,β-不饱和酮类制备 α-三氟甲基酮类。羰基化合物与二溴氟乙酸酯和三苯基膦经 Wittig 反应合成 α-氟代丙烯酸酯的促进剂。Ni 催化的与环酐的偶联反应。

訊號詞

Danger

危險分類

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

標靶器官

Central nervous system

安全危害

EUH014

儲存類別代碼

4.2 - Pyrophoric and self-heating hazardous materials

水污染物質分類（WGK）

WGK 3

閃點（°F）

44.6 °F - closed cup

閃點（°C）

7 °C - closed cup

個人防護裝備

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

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分析证书(COA)

Lot/Batch Number
SHBN6442
SHBM3091
SHBL2579
SHBJ8935
SHBJ2304

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Synthesis, 3409-3409 (2006)
Alkene-directed regioselective nickel-catalyzed cross-coupling of cyclic anhydrides with diorganozinc reagents.
Rebecca L Rogers et al.
Angewandte Chemie (International ed. in English), 46(48), 9301-9304 (2007-11-07)
Organic Syntheses, 83, 177-177 (2006)
Vincent Coeffard et al.
Organic & biomolecular chemistry, 7(8), 1723-1734 (2009-04-04)
The straightforward preparation of new modular oxazoline-containing bifunctional catalysts is reported employing a microwave-assisted Buchwald-Hartwig aryl amination as the key step. Covalent attachment of 2-(o-aminophenyl)oxazolines and pyridine derivatives generated in good-to-high yields a series of ligands in two or three
Donna K Friel et al.
Journal of the American Chemical Society, 130(30), 9942-9951 (2008-07-01)
Alkylations of pyridyl-substituted ynones with Et2Zn and Me2Zn, promoted by amino acid-based chiral ligands in the presence of Al-based alkoxides, afford tertiary propargyl alcohols efficiently in 57% to >98% ee. Two easily accessible chiral ligands are identified as optimal for
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Reagents for C–C Bond Formation

We carry a large variety of electrophiles and nucleophiles that are widely used in C–C bond-forming reactions. This group of products contains many organometallic reagents as well as commonly-used alkylating and acylating reagents.

Reagents for C–C Bond Formation

We carry a large variety of electrophiles and nucleophiles that are widely used in C–C bond-forming reactions. This group of products contains many organometallic reagents as well as commonly-used alkylating and acylating reagents.

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