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Diethylphosphine, also known as DEP, is a chemical compound with the formula (C2H5)2PH. It is a colorless, highly flammable liquid with a strong, disagreeable odor. DIETHYLPHOSPHINE is known for its reactivity and is primarily used in various chemical processes due to its unique properties.

627-49-6

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627-49-6 Usage

Uses

Used in Organic Synthesis:
Diethylphosphine is used as a reagent in organic synthesis for its ability to facilitate specific chemical reactions, contributing to the formation of desired products in the synthesis of complex organic molecules.
Used in Coordination Chemistry:
In coordination chemistry, Diethylphosphine serves as a ligand, bonding to metal centers to form coordination compounds. Its use in this field is crucial for the development of new materials with specific properties and applications.
Used in Chemical Production:
Diethylphosphine is utilized in the production of various chemical products, including pesticides and flame retardants. Its role in these applications is to provide the necessary phosphorus-based structures that contribute to the effectiveness of these products.
Used in the Production of Organic Phosphorus Compounds:
As a precursor, Diethylphosphine is used in the synthesis of other organic phosphorus compounds, which have a wide range of applications in different industries, from pharmaceuticals to agrochemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 627-49-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,2 and 7 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 627-49:
(5*6)+(4*2)+(3*7)+(2*4)+(1*9)=76
76 % 10 = 6
So 627-49-6 is a valid CAS Registry Number.
InChI:InChI=1/C4H11P/c1-3-5-4-2/h5H,3-4H2,1-2H3

627-49-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name diethylphosphane

1.2 Other means of identification

Product number -
Other names Phosphine, diethyl-

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:627-49-6 SDS

627-49-6Relevant academic research and scientific papers

PRINCIPLES OF PHOSPHORUS CHEMISTRY

Bock, Hans

, p. 3 - 53 (2007/10/02)

An up-to-date concept of bonding in phosphorus compounds has to be based on the reality of molecular states.Molecules, which change their structure with energy, at present are best rationalized in terms of topology and symmetry, effective nuclear potentials and charge distribution.To reduce the complexity of the resulting manifold, comparison of equivalent states of chemical calculations, is strongly recommended.Adding the time-scale, molecular dynamics within the numerous degrees of freedom become important, also as a basis to gain some understanding og the rather complex microscopic reaction pathways of medium-sized molecules.Examples are presented to illustrate the use of spectroscopic "fingerprints" for the analysis and optimization of gasphase reactions as well as the benefit of inherent information on molecular states for the preparative phosphorus chemist.The catalytic dehydrochlorination of alkyldichlorophosphanes RH2C-PCl2 -> RHC=PCl -> R-CP and their dechlorination on magnesium metal surface are discussed in some detail as well as the generation of other unsaturated phosphorus molecules like Cl-P=O, Cl-P=S, ClP(=O)2, Cl-P(=S)2 or H3C-P=CH2.Approximate energy hypersurface calculations for the gasphase equilibrium P4 = 2P2 or for the unexpected dehydration (H3C)2HP=O -> H2O + H3C-P=CH2, which includes chemical activation, provide some insight into microscopic reaction pathways of phosphorus compounds.

OBERFLAECHEN-REAKTIONEN 15 Heterogene Dechlorierungen von Phosphorchloriden (X)PCl3 und R-PCl2 an , , x/TiO2> und sowie spektroskopische Evidenz fuer das Entstehen von Diphospha-dicyan PC-CP aus Cl2P-CC-PCl2

Bock, H.,Bankmann, M.

, p. 167 - 191 (2007/10/02)

Stimulated by the successful generation of unsaturated molecules with low-coordinated phosphorus centers by heterogeneous surface dechlorination, Cl2P-CC-PCl2 is synthesized and characterized by PE and mass spectra.In addition, curls, wool and catalysts x/TiO2> or are tested as potential dechlorinating agents for phosphorus halides like OPCl3, SPCl3, H3C-PCl2, H5C2-PCl2, (H3C)3C-PCl2 or H5C6-PCl2 in a gasflow reactor under reduced pressure and yield, inter alia, the following representative results: due to the thermodynamically favored formation of , or at the Mg surface, P4 is the only gaseous product identified from reactions of OPCl3 and SPCl3 with metal at higher temperatures.On the contrary, passing H3C-PCl2 at 600K over yields a reaction mixture containing P(CH3)3, (H3C)2P-P(CH3)2 (H3C-P)5 and CH4, which suggests an intermediate formation of surface phosphinidenes Mg>.Analogously, the pentamer (H3C-H2C-P)5 can be isolated from ethyldichlorophosphane.Reaction of the evaporated diphospha-cyanogen precursor Cl2P-C-PCl2 with the catalyst produces predominantly PCl3, and P4, but PE and mass spectra provide evidence that also minor amounts of the hitherto unknown molecule PC-CP are formed.

Evidence for Surface Phosphinidene Intermediates Mg> in the Heterogeneous Dechlorination of Alkyldichlorophosphanes RPCl2 by Mg Metal

Bock, Hans,Bankmann, Martin

, p. 1130 - 1132 (2007/10/02)

The heterogeneous dechlorination of alkyldichlorophosphanes by Mg metal at 600 K yields chemisorbed products which include penta-alkylcyclopentaphosphanes (RP)5, in addition to RnPH(3-n), R2P-PR2, P4, RH, and R-R, and thus provides evidence for surface phosphinidene intermediates Mg>.

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