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925253-65-2

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925253-65-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 925253-65-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,5,2,5 and 3 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 925253-65:
(8*9)+(7*2)+(6*5)+(5*2)+(4*5)+(3*3)+(2*6)+(1*5)=172
172 % 10 = 2
So 925253-65-2 is a valid CAS Registry Number.

925253-65-2Downstream Products

925253-65-2Relevant academic research and scientific papers

Mild and Efficient Synthesis of Diverse Organo-AuI-L Complexes in Green Solvents

Ingner, Fredric J. L.,Schmitt, Ann-Cathrin,Orthaber, Andreas,Gates, Paul J.,Pilarski, Lukasz T.

, p. 2032 - 2037 (2020/03/11)

An exceptionally mild and efficient method was developed for the preparation of (hetero)aryl-AuI-L complexes using ethanol or water as the reaction medium at room temperature and Ar-B(triol)K boronates as the transmetalation partner. The reaction does not need an exogeneous base or other additives, and quantitative yields can be achieved through a simple filtration as the only required purification method, which obviates considerable waste associated with alternative workup methods. A broad reaction scope was demonstrated with respect to both the L and (hetero)aryl ligands on product Au complexes. Despite the polar reaction medium, large polycyclic aromatic hydrocarbon units can be incorporated on the Au complexes in very good to excellent yields. The approach was demonstrated for the chemoselective manipulation of orthogonally protected aryl boronates to afford a new class of N-heterocyclic carbene-Au-aryl complexes. A mechanistic rationale was proposed.

Stille coupling involving bulky groups feasible with gold cocatalyst

Delpozo, Juan,Carrasco, Desiree,Perez-Temprano, Monica H.,Garcia-Melchor, Max,Alvarez, Rosana,Casares, Juan A.,Espinet, Pablo

, p. 2189 - 2193 (2013/04/10)

Gold shuttle: Bulky groups, which will not (or only very sluggishly) undergo Stille coupling with stannanes and inexpensive ligands, can be efficiently coupled using bimetallic catalysis. A gold cocatalyst serves as an efficient shuttle to convey the bulky group from tin to palladium by reducing the steric crowding in the transition-states (see scheme). Copyright

Relativistic functional groups: Aryl carbon-gold bond formation by selective transmetalation of boronic acids

Partyka, David V.,Zeller, Matthias,Hunter, Allen D.,Gray, Thomas G.

, p. 8188 - 8191 (2008/02/02)

(Chemical Equation Presented) Gilded organometallics: Carbon-gold bond formation occurs selectively and in high yields upon reaction of gold(I) bromides with arylboronic acids in the presence of Cs2CO3. The reaction is broadly tolera

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