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Benzenamine, 4-(diethylphosphino)-N,N-dimethyl-, also known as 4-Diethylphosphino-N,N-dimethylaniline, is a phosphine ligand with a unique structure that features a benzene ring, an amine group, and a diethylphosphino group. This chemical compound is widely used in coordination chemistry and organometallic chemistry due to its strong coordinating ability and stability. Its versatile applications in various industries, including pharmaceutical, agrochemical, material science, and catalysis, make it a valuable compound in chemical research and development.

17005-57-1

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17005-57-1 Usage

Uses

Used in Pharmaceutical Industry:
Benzenamine, 4-(diethylphosphino)-N,N-dimethylis used as a catalyst in the synthesis of complex organic molecules, particularly in the pharmaceutical industry. Its ability to coordinate with metal ions makes it a valuable component in the development of new drugs and drug delivery systems.
Used in Agrochemical Industry:
In the agrochemical industry, Benzenamine, 4-(diethylphosphino)-N,N-dimethylis employed as a catalyst in the production of various agrochemicals, such as pesticides and herbicides. Its strong coordinating ability allows for the efficient synthesis of these compounds, contributing to the development of more effective and environmentally friendly products.
Used in Material Science:
Benzenamine, 4-(diethylphosphino)-N,N-dimethylis utilized in material science for the development of advanced materials with unique properties. Its coordination chemistry allows for the creation of new materials with improved performance in areas such as electronics, sensors, and energy storage.
Used in Catalysis:
In the field of catalysis, Benzenamine, 4-(diethylphosphino)-N,N-dimethylis used as a catalyst in various chemical reactions. Its strong coordinating ability and stability make it an effective catalyst for a wide range of reactions, including hydrogenation, hydroformylation, and carbon-carbon bond formation. This contributes to the development of more efficient and environmentally friendly catalytic processes.
Overall, Benzenamine, 4-(diethylphosphino)-N,N-dimethylis a versatile and valuable compound with a wide range of applications across different industries. Its unique structure and properties make it an essential component in the development of new technologies and products in the fields of pharmaceuticals, agrochemicals, material science, and catalysis.

Check Digit Verification of cas no

The CAS Registry Mumber 17005-57-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,0,0 and 5 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 17005-57:
(7*1)+(6*7)+(5*0)+(4*0)+(3*5)+(2*5)+(1*7)=81
81 % 10 = 1
So 17005-57-1 is a valid CAS Registry Number.

17005-57-1 Well-known Company Product Price

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  • Aldrich

  • (747270)  4-(Diethylphosphino)-N,N-dimethylaniline  97%

  • 17005-57-1

  • 747270-1G

  • 1,191.06CNY

  • Detail
  • Aldrich

  • (747270)  4-(Diethylphosphino)-N,N-dimethylaniline  97%

  • 17005-57-1

  • 747270-5G

  • 5,268.51CNY

  • Detail

17005-57-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-diethylphosphanyl-N,N-dimethylaniline

1.2 Other means of identification

Product number -
Other names Benzenamine,4-(diethylphosphino)-N,N-dimethyl

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:17005-57-1 SDS

17005-57-1Relevant academic research and scientific papers

Synthesis of dihydropyridines and pyridines from imines and alkynes via C-H activation

Colby, Denise A.,Bergman, Robert G.,Ellman, Jonathan A.

, p. 3645 - 3651 (2008/10/09)

A convenient one-pot C-H alkenylation/electrocyclization/aromatization sequence has been developed for the synthesis of highly substituted pyridine derivatives from alkynes and α,β-unsaturated N-benzyl aldimines and ketimines that proceeds through dihydropyridine intermediates. A new class of ligands for C-H activation was developed, providing broader scope for the alkenylation step than could be achieved with previously reported ligands. Substantial information was obtained about the mechanism of the reaction. This included the isolation of a C-H activated complex and its structure determination by X-ray analysis; in addition, kinetic simulations using the Copasi software were employed to determine rate constants for this transformation, implicating facile C-H oxidative addition and slow reductive elimination steps.

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