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1233717-68-4

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1233717-68-4 Usage

Reaction

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

Uses

Bis[di-tert-butyl(4-dimethylaminophenyl)phosphine]palladium(0) is used in cross-coupling including sp2-sp3 coupling, especially Suzuki, Negishi-type, Heck, Sonogashira, and Buchwald-Hartwig coupling reactions.

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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  • (Code)Product description
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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 articles and documents

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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