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Bis[di-tert-butyl(4-dimethylaminophenyl)phosphine]palladium(0), Pd 16.7%, is a homogeneous palladium catalyst with a unique structure that features two di-tert-butyl(4-dimethylaminophenyl)phosphine ligands. Bis[di-tert-butyl(4-diMethylaMinophenyl)phosphine]palladiuM(0), Pd 16.7% is characterized by its high purity and palladium content, making it a highly effective catalyst for various cross-coupling reactions in organic synthesis.

1233717-68-4

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1233717-68-4 Usage

Uses

Used in Pharmaceutical Industry:
Bis[di-tert-butyl(4-dimethylaminophenyl)phosphine]palladium(0), Pd 16.7%, is used as a catalyst for cross-coupling reactions in the synthesis of complex organic molecules, including pharmaceutical compounds. Its high purity and palladium content contribute to the efficient formation of desired products, reducing side reactions and improving overall yields.
Used in Chemical Industry:
In the chemical industry, Bis[di-tert-butyl(4-dimethylaminophenyl)phosphine]palladium(0), Pd 16.7%, is used as a catalyst for sp2-sp3 coupling reactions, including Suzuki, Negishi-type, Heck, Sonogashira, and Buchwald-Hartwig coupling reactions. These reactions are essential for the synthesis of various organic compounds, such as polymers, dyes, and specialty chemicals.
Used in Research and Development:
Bis[di-tert-butyl(4-dimethylaminophenyl)phosphine]palladium(0), Pd 16.7%, is utilized in research and development settings for the investigation of new cross-coupling reactions and the optimization of existing ones. Its high purity and palladium content make it an ideal catalyst for exploring novel synthetic routes and improving reaction conditions.

Reaction

Catalyst used for the Heck alkynylation of aryl and heteroaryl chlorides.

Check Digit Verification of cas no

The CAS Registry Mumber 1233717-68-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,3,3,7,1 and 7 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1233717-68:
(9*1)+(8*2)+(7*3)+(6*3)+(5*7)+(4*1)+(3*7)+(2*6)+(1*8)=144
144 % 10 = 4
So 1233717-68-4 is a valid CAS Registry Number.

1233717-68-4 Well-known Company Product Price

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  • Alfa Aesar

  • (46000)  Bis[di-tert-butyl(4-dimethylaminophenyl)phosphine]palladium(0), Pd 16.7%   

  • 1233717-68-4

  • 250mg

  • 1208.0CNY

  • Detail
  • Alfa Aesar

  • (46000)  Bis[di-tert-butyl(4-dimethylaminophenyl)phosphine]palladium(0), Pd 16.7%   

  • 1233717-68-4

  • 1g

  • 3859.0CNY

  • Detail

1233717-68-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name [t-Bu2(4-Me2NC6H4)P]2Pd

1.2 Other means of identification

Product number -
Other names BIS{[4-(N,N-DIMETHYLAMINO)PHENYL]DI-T-BUTYLPHOSPHINO}PALLADIUM(0)

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:1233717-68-4 SDS

1233717-68-4Downstream Products

1233717-68-4Relevant academic research and scientific papers

The impact of palladium(II) Reduction pathways on the structure and activity of palladium(0) catalysts

Wei, Carolyn S.,Davies, Geraint H. M.,Soltani, Omid,Albrecht, Jacob,Gao, Qi,Pathirana, Charles,Hsiao, Yi,Tummala, Srinivas,Eastgate, Martin D.

, p. 5822 - 5826 (2013/07/11)

Two roads diverged: The mechanism of insitu PdII catalyst activation to generate an active {LnPd0} catalyst from an air-stable PdII precursor was examined using the standard conditions of a Miyaura borylation reaction. Two pathways for catalyst activation exist under these conditions, producing two structurally and chemically distinct {LnPd0} complexes (see scheme). Copyright

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