406023
二乙基锌 溶液
1.0 M in heptane
别名:
Zincdiethyl
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关于此项目
线性分子式:
(C2H5)2Zn
化学文摘社编号:
分子量:
123.51
UNSPSC Code:
12352103
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
3587207
产品名称
二乙基锌 溶液, 1.0 M in heptane
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
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Application
二乙基锌溶液可用于合成：
- 双（吡啶基吡咯基）锌发光配合物。
- 通用构件块，5-（酮芳基）噻唑。
- 具有高发光性能的 ZnxCd1-xSe 纳米晶体。
signalword
Danger
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
target_organs
Central nervous system
supp_hazards
存储类别
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
法规信息
危险化学品
此项目有
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)
Su-Xi Wang et al.
Chemical & pharmaceutical bulletin, 55(7), 1011-1013 (2007-07-03)
Newly synthesized polymer-supported chiral amino alcohol catalysts 5a and 5b have been proved to be effective for the enantioselective addition of diethylzinc to aldehydes, affording the corresponding sec-alcohols in moderate enantiomeric excesses with good to excellent yields. The recycled catalyst
Yan Yin et al.
The Journal of organic chemistry, 72(15), 5731-5736 (2007-06-22)
Intramolecular hydroamination of alkynyl amides was effected by a catalytic amount of Et2Zn (20 mol %) to form indole derivatives, and a tandem cyclization/nucleophilic addition procedure involving reaction of the indole zinc salt intermediate with acid chlorides or halides was
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