跳转至内容
Merck
CN

253189

三(二乙氨基)膦

97%, liquid

别名:

三（N,N-二乙氨基）膦, 三（二乙基氨基）膦, 亚磷酸三（二乙酰胺）, 六乙基三氨基磷酸酯, 六乙基三胺磷, 六乙基亚磷酰三胺

登录 查看组织和合同定价。

选择尺寸

关于此项目

线性分子式:
P[N(C2H5)2]3
化学文摘社编号:
2283-11-6
分子量:
247.36
NACRES:
NA.22
PubChem Substance ID:
24855300
UNSPSC Code:
12352001
EC Number:
218-920-8
MDL number:
MFCD00009041
Beilstein/REAXYS Number:
636187

主要文件

查看所有文档
技术服务
需要帮助？我们经验丰富的科学家团队随时乐意为您服务。
让我们为您提供帮助
技术服务
需要帮助？我们经验丰富的科学家团队随时乐意为您服务。
让我们为您提供帮助

产品名称

三(二乙氨基)膦, 97%

InChI key

FDIOSTIIZGWENY-UHFFFAOYSA-N

InChI

1S/C12H30N3P/c1-7-13(8-2)16(14(9-3)10-4)15(11-5)12-6/h7-12H2,1-6H3

SMILES string

CCN(CC)P(N(CC)CC)N(CC)CC

assay

97%

form

liquid

reaction suitability

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

Quality Level

200

bp

80-90 °C/10 mmHg (lit.)

density

0.903 g/mL at 25 °C (lit.)

functional group

phosphine

相关类别

Application

三（二乙氨基）膦[(Et2N)3P]可作为试剂，合成以下物质：
  • 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。

pictograms

FlameExclamation mark
GHS02,GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

存储类别

3 - Flammable liquids

flash_point_f

138.2 °F - closed cup

flash_point_c

59 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

法规信息

危险化学品
此项目有

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
BCCK2816
BCBW8214
BCBQ4295V
BCBM2490V
SHBD3132V

没有发现合适的版本？

如果您需要特殊版本，可通过批号或批次号查找具体证书。

搜索COA

已有该产品？

在文件库中查找您最近购买产品的文档。

访问文档库

Khadga J Karki et al.
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
Bogdanov AV, et al.
Synthesis, 2010(19), 3268- 3270 (2010)
Novel 1-Aminomethylisatins: Peculiarities of the Synthesis and the Reaction with Tris (diethylamino) phosphine
Bogdanov AV, et al.
Journal of Heterocyclic Chemistry, 51(4), 1027- 1030 (2014)
K Yamana et al.
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.
Irina P Romanova et al.
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
查看所有相关文献

相关内容

Catalexis 催化剂筛选

Catalexis平台通过数字化优化催化剂筛选，识别出交叉偶联反应最有效的膦配体，从而增强催化作用。

Phosphine Ligand Application Guide

Phosphine Ligand Application Guide

Catalyst Screening with Catalexis

The Catalexis platform enhances catalysis by digitally optimizing catalyst selection to identify the most effective phosphine ligands for cross-coupling reactions.

我们的科学家团队拥有各种研究领域经验，包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.

联系客户支持