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BIS(DIISOPROPYLAMINO)-PHOSPHINE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

68880-43-3

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68880-43-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 68880-43-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,8,8 and 0 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 68880-43:
(7*6)+(6*8)+(5*8)+(4*8)+(3*0)+(2*4)+(1*3)=173
173 % 10 = 3
So 68880-43-3 is a valid CAS Registry Number.

68880-43-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[di(propan-2-yl)amino]phosphanyl-N-propan-2-ylpropan-2-amine

1.2 Other means of identification

Product number -
Other names -

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:68880-43-3 SDS

68880-43-3Downstream Products

68880-43-3Relevant academic research and scientific papers

15N Nuclear Magnetic Resonance Study of Two-Coordinate Phosphorus Cations - Sign-Determination of Coupling Constants - Application of Two-Dimensional (2D) Heteronuclear Shift Correlations

Wrackmeyer, Bernd,Schiller, Juergen

, p. 662 - 667 (2007/10/02)

Key Words: Phosphenium Cations, 31P NMR, 13C NMR, 15N NMR, 29Si NMR Cyclic and non-cyclic bis(amino)phosphenium cations (1 to 4) together with their precursors (bis(amino)phosphorus chlorides 5 to 8) and some other bis(amino)phosphorus compounds (9 to 14) have been studied by 13C, 15N (natural abundance), 29Si and 31P NMR spectroscopy. 15N chemical shifts and coupling constants 1J(31P15N) of phosphenium cations have been determined for the first time.NMR data of 1 to 4 are compared with those of a bis(amino)carbene and various bis(amino)stannylenes.In the phosphenium cations 1 to 4 the 15N nuclear shielding is considerably reduced (ca. 70 to 100 ppm as compared with 5 to 14) and there is a crude linear relationship between δ15N and δ31P values.Changes in the δ15N values of 1 to 4 do not reflect P-N (pp)? interactions.A positive sign has been determined for the coupling constants 1J(31P15N) 1K(31P15N) for the phosphenium cations and for all other P(III)-N compounds studied.This was achieved by applying various one- and twodimensional heteronuclear double resonance techniques.The experiments also gave signs of the coupling constants 2J(31PN13C), 2J(31PN29Si), 3J(31PNC13C), 3J(31PNSi13C), 4J(31PNCC1H) and 4J(31PNSiC1H).Negative contributions to 1K(31P15N), arising from the lone pair of electrons at phosphorus, are more noticeable in the case of the phosphenium cations.

Redox Properties of Diphosphanes

Niemann, Juergen,Schoeller, Wolfgang W.,Goenna, Volker von der,Niecke, Edgar

, p. 1563 - 1565 (2007/10/02)

Diphosphanes undergo electrochemical one-electron oxidation.In case amino groups are at the phosphorus, the resulting distonic diphosphane radical cations disproportionate readily into a dication and a diphosphane; the former separates into two phosphenium cations. Key Words: Diphosphanes / Cyclic voltammetry / Calculations, MNDO, ab initio

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