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88345-93-1

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88345-93-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88345-93-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,3,4 and 5 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 88345-93:
(7*8)+(6*8)+(5*3)+(4*4)+(3*5)+(2*9)+(1*3)=171
171 % 10 = 1
So 88345-93-1 is a valid CAS Registry Number.

88345-93-1Relevant articles and documents

Cyclotriveratrylene-tethered trinuclear palladium(ii)-NHC complexes; Reversal of site selectivity in Suzuki-Miyaura reactions

Fowler, Jonathan M.,Britton, Edward,Pask, Christopher M.,Willans, Charlotte E.,Hardie, Michaele J.

, p. 14687 - 14695 (2019)

The trinuclear complexes [{PdI2(pyCl)}3(L1)] C1 and [{PdI2(pyCl)}3(L2)] C2, where pyCl = 3-chloropyridine, L1 = methyl(cyclotriguaiacylenyl)methylbenzimidazol-2-ylidene and L2 = benzyl(cyclotriguaiacylenyl)methy

Selective palladium-catalysed arylation of 2,6-dibromopyridine using N-heterocyclic carbene ligands

Prajapati,Schulzke,Kindermann,Kapdi

, p. 53073 - 53085 (2015/06/25)

A selective palladium-catalysed arylation of 2,6-dibromopyridine has been developed by employing N-heterocyclic carbene ligands. Selective mono-arylation was performed in water/acetonitrile solvent system at ambient temperature with catalyst loading of 0.1 mol%. This reaction was also found to proceed smoothly in water although at a slightly elevated temperature of 80 °C. 2,6-Disubstituted and diversely substituted 2,6-pyridines were also obtained in high yields which will be of importance to organic and medicinal chemists.

Triarylbismuthanes as threefold aryl-transfer reagents in regioselective cross-coupling reactions with bromopyridines and quinolines

Rao, Maddali L.N.,Dhanorkar, Ritesh J.

supporting information, p. 5214 - 5228 (2014/10/15)

Cross-coupling studies using bromopyridines and bromoquinolines with triarylbismuths as threefold coupling reagents in substoichiometric amounts under Pd-catalysed conditions are disclosed. The reactivity was high with both mono- and dibromopyridyl substrates, and mono- and bis-couplings were carried out regioselectively. A library of monoaryl and diaryl pyridines was formed in high yields. A one-pot strategy provided a simple and straightforward synthesis of both symmetrical and unsymmetrical diarylpyridines. Arylations of 2-bromo- and 3-bromoquinolines were achieved with triarylbismuth reagents. This study demonstrates that triarylbismuths may be used as threefold arylating reagents for the synthesis of aryl pyridines and quinolines through couplings with bromopyridines and bromoquinolines under Pd-catalysed conditions. Copyright

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