245275
三乙基膦
99%, liquid
别名:
Triethylphosphorus
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关于此项目
线性分子式:
(C2H5)3P
化学文摘社编号:
分子量:
118.16
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352128
EC Number:
209-068-8
MDL number:
Beilstein/REAXYS Number:
969170
产品名称
三乙基膦, 99%
InChI key
RXJKFRMDXUJTEX-UHFFFAOYSA-N
InChI
1S/C6H15P/c1-4-7(5-2)6-3/h4-6H2,1-3H3
SMILES string
CCP(CC)CC
assay
99%
form
liquid
reaction suitability
reagent type: ligand
reaction type: Arylations
refractive index
n20/D 1.456 (lit.)
bp
127-128 °C (lit.)
density
0.802 g/mL at 20 °C (lit.)
functional group
phosphine
Quality Level
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Application
Triethylphosphine is generally used as a ligand in the organometallic chemistry. It can be used in:
- Synthesis of the tetrahedrally coordinated L3Fe-Nx complex with a terminal nitride group.
- Synthesis of (PEt3)2Ni(η2-C14H10), a source of the reactive Ni(PEt3)2 moiety.
- Synthesis of dinuclear rhodium complexes with triethyllphosphane bridges.
Other Notes
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signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Pyr. Liq. 1 - Skin Corr. 1B
存储类别
4.2 - Pyrophoric and self-heating hazardous materials
wgk
WGK 3
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
法规信息
新产品
此项目有
A Tetrahedrally Coordinated L3Fe? N x Platform that Accommodates Terminal Nitride (FeIV? N) and Dinitrogen (FeI? N2? FeI) Ligands.
Betley T A and Peters J C
Journal of the American Chemical Society, 126(20), 6252-6254 (2004)
Unexpected Intermediates and Products in the C? F Bond Activation of Tetrafluorobenzenes with a Bis (triethylphosphine) Nickel Synthon: Direct Evidence of a Rapid and Reversible C? H Bond Activation by Ni (0).
Johnson S A, et al.
Journal of the American Chemical Society, 130(51), 17278-17280 (2008)
Breaking the Rule: Synthesis and Molecular Structure of Dinuclear Rhodium Complexes with Bridging and Semibridging Trialkylphosphane Ligands.
Pechmann T, et al.
Angewandte Chemie (International Edition in English), 39(21), 3909-3911 (2000)
Matthew R Richardson et al.
Proteomics, 9(9), 2468-2483 (2009-04-30)
Although low-density lipoprotein (LDL) plays a predominant role in atherogenesis, the low-density lipoproteome has not been fully characterized. Moreover, alterations from a Western diet, diabetes, and physical inactivity on this proteome have yet to be determined. Accordingly, relative quantification was
Sarah A Weicker et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 21(37), 13027-13034 (2015-08-01)
Silyl triflates of the form R4-n Si(OTf)n (n=1, 2; OTf=OSO3 CF3 ) are shown to activate carbon dioxide when paired with bulky alkyl-substituted Group 15 bases. Combinations of silyl triflates and 2,2,6,6-tetramethylpiperidine react with CO2 to afford silyl carbamates via a
相关内容
Phosphine Ligand Application Guide
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