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Benzenamine, 4-(diphenylphosphinothioyl)-N,N-dimethyl- is a chemical compound with the molecular formula C18H18NPS. It is a derivative of aniline, where the hydrogen atom at the 4-position is replaced by a diphenylphosphinothioyl group, and the two remaining hydrogen atoms on the nitrogen atom are replaced by methyl groups. Benzenamine, 4-(diphenylphosphinothioyl)-N,N-dimethyl- is an example of a phosphine sulfide, which is a type of organophosphorus compound. It is often used as a ligand in coordination chemistry, particularly in the formation of transition metal complexes. The compound is known for its potential applications in catalysis and as a precursor in the synthesis of various pharmaceuticals and agrochemicals. Its chemical structure provides it with unique electronic and steric properties, making it a valuable building block in the development of new materials and compounds.

1041-99-2

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1041-99-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1041-99-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,4 and 1 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1041-99:
(6*1)+(5*0)+(4*4)+(3*1)+(2*9)+(1*9)=52
52 % 10 = 2
So 1041-99-2 is a valid CAS Registry Number.

1041-99-2SDS

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 4-diphenylthiophosphinoyl-N,N-dimethyl-aniline

1.2 Other means of identification

Product number -
Other names [4-(Diphenyl-phosphinothioyl)-phenyl]-dimethyl-amine

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:1041-99-2 SDS

1041-99-2Downstream Products

1041-99-2Relevant academic research and scientific papers

The Kinetics and Mechanism of the Reaction of Tricoordinate Phosphorus Compounds with Diaryl Trisulfides

Hall, C. Dennis,Tweedy, Bruce R.,Kayhanian, Robert,Lloyd, John R.

, p. 775 - 779 (2007/10/02)

Kinetic data and activation parameters are reported for the reaction of a series of tricoordinate phosphorus compounds, , with diaryl trisulfides.The second-order rate coefficients for series of arylphosphines, phosphinites and phosphonites, correlate with the Hammett ? constants of the aryl substituents with ρ values of -1.1, -1.1 and -1.1 respectively and these results are discussed in terms of a biphilic mechanism analogous to that proposed for the reaction of tricoordinate phosphorus with S8.

Kinetics and mechanism of the reaction of trico-ordinate phosphorus ompounds with octasulphur

Lloyd, John R.,Lowther, Nicholas,Zsabo, G.,Hall, C. Dennis

, p. 1813 - 1818 (2007/10/02)

Kinetic data and activation parameters are reported for the reactions of a series of phosphites, arylphosphonites, diarylphosphinites, and triarylphosphines with octasulphur (S8) in toluene as solvent.For the phosphites the data are explained in terms of changes in p-character of the Ione-pair orbital on phosphorus and inductive electron donation by the alkyl groups.The rates of reaction of series of arylphosphonites, diarylphosphonites, and triarylphosphones correlate with the Hammett ? constants to give ? values of -3.0, -3.0, and -2.5, respactively, and the results are discussed in terms of the Reactivity-Selectivity Principle and the biphilic mechanism or insertion of trico-ordinate phosphorus into ?-bonds.

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