12131-44-1 Usage
Description
Di-chlorobis[(1,2,3-)-1-phenyl-2-propenyl]dipalladium(II), 98% is a transition metal complex that serves as an essential reagent in various organic syntheses. It is a catalyst for ammonia cross-coupling reactions and the conversion of aryl triflates to fluorides, making it a valuable component in the field of organic chemistry.
Uses
Used in Pharmaceutical Industry:
Di-chlorobis[(1,2,3-)-1-phenyl-2-propenyl]dipalladium(II), 98% is used as a catalyst for the synthesis of arylamines, which are essential building blocks in the development of various pharmaceutical compounds. The application reason is to facilitate the formation of arylamines through ammonia cross-coupling reactions, contributing to the production of new and effective drugs.
Used in Chemical Industry:
In the chemical industry, Di-chlorobis[(1,2,3-)-1-phenyl-2-propenyl]dipalladium(II), 98% is used as a catalyst for the conversion of aryl triflates to fluorides. This application is crucial for the synthesis of various organic compounds, including those used in the production of agrochemicals, dyes, and other specialty chemicals.
Used in Research and Development:
Di-chlorobis[(1,2,3-)-1-phenyl-2-propenyl]dipalladium(II), 98% is also used as an important reagent in research and development for the exploration of new synthetic pathways and the development of novel chemical compounds. The application reason is to enable the discovery of new reactions and improve the efficiency of existing synthetic methods, ultimately leading to the creation of innovative products and materials.
Reaction
Precursor for the preparation of a palladium catalyst used in the carbonylative arylation of ketones, yielding vinylbenzoate compounds.
Precursor for the preparation of a palladium catalyst used in the Buchwald-Hartwig amination of (hetero)aryl chlorides.
Precursor for the preparation of a palladium catalyst used in the arylative dearomatization of phenols.
Versatile palladium precursor for the preparation of palladium catalysts used in the cross-coupling of aryl chlorides and amines , conversion of aryl triflates to aryl fluorides , and the α-arylation of aldehydes .
Check Digit Verification of cas no
The CAS Registry Mumber 12131-44-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,2,1,3 and 1 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 12131-44:
(7*1)+(6*2)+(5*1)+(4*3)+(3*1)+(2*4)+(1*4)=51
51 % 10 = 1
So 12131-44-1 is a valid CAS Registry Number.
