59211-64-2 Usage
General Description
[1,1'-Biphenyl]-4-carbonitrile, 4'-acetyl- is a chemical compound with a molecular formula of C16H11N. It is a derivative of biphenyl, which is a type of organic compound commonly used in the production of various industrial chemicals and consumer products. The addition of the acetyl group at the 4' position modifies the chemical properties of the biphenyl molecule, potentially affecting its reactivity and solubility in different solvents. [1,1'-Biphenyl]-4-carbonitrile, 4'-acetyl- may have various potential applications in the field of chemical synthesis, materials science, and pharmaceutical research. However, further research and testing are needed to fully understand its properties and potential uses.
Check Digit Verification of cas no
The CAS Registry Mumber 59211-64-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,2,1 and 1 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 59211-64:
(7*5)+(6*9)+(5*2)+(4*1)+(3*1)+(2*6)+(1*4)=122
122 % 10 = 2
So 59211-64-2 is a valid CAS Registry Number.
59211-64-2Relevant articles and documents
Polymer-Assisted Solution-Phase (PASP) Suzuki Couplings Employing an Anthracene-Tagged Palladium Catalyst
Lan, Ping,Berta, Daniela,Porco Jr., John A.,South, Michael S.,Parlow, John J.
, p. 9678 - 9686 (2007/10/03)
A general method for polymer-assisted solution-phase (PASP) Suzuki reactions employing a combination of anthracene-tagged palladium catalyst and anthracene-tagged boronic acid with a polymer-supported carbonate base is reported. The anthracene-tagged catalyst allows for the easy removal of the Pd catalyst along with the dissociated phosphine ligand and phosphine oxide byproducts by sequestration through a chemoselective Diels-Alder reaction with a maleimide resin. The polymer-supported carbonate base facilitates the removal of excess boronic acid and the borane-containing byproducts present at the end of the coupling reaction. The Suzuki coupling reaction can be efficiently conducted by using combinations of the anthracene-tagged Pd catalyst, polymer-supported carbonate base, and anthracene-tagged boronic acid to yield the desired product in high purity and yield without the use of chromatography.
