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品質等級
化驗
97%
形狀
liquid
反應適用性
reaction type: Buchwald-Hartwig Cross Coupling Reaction
reaction type: Heck Reaction
reaction type: Hiyama Coupling
reaction type: Negishi Coupling
reaction type: Sonogashira Coupling
reaction type: Stille Coupling
reaction type: Suzuki-Miyaura Coupling
reagent type: ligand
折射率
n20/D 1.475 (lit.)
bp
80-90 °C/10 mmHg (lit.)
密度
0.903 g/mL at 25 °C (lit.)
官能基
phosphine
SMILES 字串
CCN(CC)P(N(CC)CC)N(CC)CC
InChI
1S/C12H30N3P/c1-7-13(8-2)16(14(9-3)10-4)15(11-5)12-6/h7-12H2,1-6H3
InChI 密鑰
FDIOSTIIZGWENY-UHFFFAOYSA-N
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應用
三(二乙氨基)膦[(Et2N)3P]可作为试剂,合成以下物质:
也可用于通过富勒烯C60对某些环状 α-二酮进行脱氧。
- 1,1′-二烷基异靛蓝衍生物,通过脱氧反应与各种1-烷基异丁烯反应进行合成。
- 1-氨基甲基靛红,通过靛红与伯胺和仲胺反应合成。
也可用于通过富勒烯C60对某些环状 α-二酮进行脱氧。
訊號詞
Warning
危險分類
Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3
標靶器官
Respiratory system
儲存類別代碼
3 - Flammable liquids
水污染物質分類(WGK)
WGK 3
閃點(°F)
138.2 °F - closed cup
閃點(°C)
59 °C - closed cup
個人防護裝備
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
其他客户在看
Scientific reports, 3, 2287-2287 (2013-07-28)
Multiple exciton generation (MEG) is a process in which more than one exciton is generated upon the absorption of a high energy photon, typically higher than two times the band gap, in semiconductor nanocrystals. It can be observed experimentally using
Facile synthesis of 1, 1′-dialkylisoindigos through deoxygenation reaction of isatins and tris (diethylamino) phosphine
Synthesis, 2010(19), 3268- 3270 (2010)
Novel 1-Aminomethylisatins: Peculiarities of the Synthesis and the Reaction with Tris (diethylamino) phosphine
Journal of Heterocyclic Chemistry, 51(4), 1027- 1030 (2014)
The Journal of organic chemistry, 76(8), 2548-2557 (2011-03-12)
The reactions of such cyclic α-diketones as acenaphthenequinone, aceanthrenequinone, and N-alkylisatins, with hexaethyltriaminophosphine in the presence of the fullerene C(60), lead to the formation of methanofullerene derivatives under mild conditions. This process proceeds via deoxygenation of the dicarbonyl compound by
Nucleic acids symposium series, (21)(21), 31-32 (1989-01-01)
Utilities of deoxyribonucleoside 3'-O-phosphorbisdiethylamidites in the synthesis of oligodeoxyribonucleotides and their analogues are described.
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