推荐产品
方案
98%
表单
liquid
折射率
n20/D 1.4343 (lit.)
沸点
189-192 °C (lit.)
密度
0.808 g/mL at 25 °C (lit.)
官能团
amine
SMILES字符串
CCN(CC)CCN(CC)CC
InChI
1S/C10H24N2/c1-5-11(6-2)9-10-12(7-3)8-4/h5-10H2,1-4H3
InChI key
DIHKMUNUGQVFES-UHFFFAOYSA-N
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应用
N,N, N′,N′-Tetraethylethylenediamine (TEEDA) has been used in the synthesis of amine ligands using simple or double intramolecular dealkylation reaction. TEEDA exhibits selective β-lithiation during deprotonation with lithiumalkyls.
警示用语：
Danger
危险分类
Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1B
储存分类代码
3 - Flammable liquids
WGK
WGK 1
闪点(°F)
138.2 °F - closed cup
闪点(°C)
59 °C - closed cup
个人防护装备
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
法规信息
危险化学品
从最新的版本中选择一种：
分析证书(COA)
Lot/Batch Number
M Esther Morilla et al.
Chemical communications (Cambridge, England), (17)(17), 1848-1849 (2002-09-26)
N,N, N',N'-Tetraethylethylenediamine undergoes simple or double intramolecular dealkylation reactions in the presence of the complexes [RuCl2(diene)]n (diene = cod, nbd) or trans-[RuCl2(diene)(morfoline)2 at 80 degrees C to afford chelating amine ligands which contains one or two N-H functionalities.
Viktoria H Gessner et al.
Journal of the American Chemical Society, 130(44), 14412-14413 (2008-10-10)
TMEDA and its ethyl-substituted analogue, TEEDA, show a different behavior toward the deprotonation with lithiumalkyls. While TMEDA mainly undergoes alpha-lithiation of its methyl group, TEEDA shows selective beta-lithiation with following elimination of ethene. The crystal structure of the monomeric intermediate
Wei Xiao et al.
Biochimica et biophysica acta. General subjects, 1862(8), 1760-1769 (2018-05-12)
The inorganic core of the iron storage protein, ferritin, is recognized as being analogous to the poorly crystalline iron mineral, ferrihydrite (Fh). Fh is also abundant in soils where it is central to the redox cycling of particular soil contaminants
Lan-Fang Hu et al.
Molecules (Basel, Switzerland), 25(2) (2020-01-16)
The copolymerization of biorenewable succinic anhydride (SA) with propylene oxide (PO) is a promising way to synthesize biodegradable aliphatic polyesters. However, the catalytic systems for this reaction still deserve to be explored because the catalytic activity of the reported catalysts
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