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dimethyl 3,3'-(pyridine-2,6-diyl)dibenzoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1258419-84-9

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1258419-84-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1258419-84-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,8,4,1 and 9 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1258419-84:
(9*1)+(8*2)+(7*5)+(6*8)+(5*4)+(4*1)+(3*9)+(2*8)+(1*4)=179
179 % 10 = 9
So 1258419-84-9 is a valid CAS Registry Number.

1258419-84-9Relevant academic research and scientific papers

Synthesis and characterization of low-nuclearity lantern-type porous coordination cages

Taggart, Garrett A.,Lorzing, Gregory R.,Dworzak, Michael R.,Yap, Glenn P. A.,Bloch, Eric D.

supporting information, p. 8924 - 8927 (2020/08/17)

Permanent porosity in lantern-type M4L4 paddlewheel-based cages is rare and has only been reported for naphthalene, naphthyridine, and diethynylbenzene-based linkers. This work presents the design, synthesis, and characterization of small lanterns that ex

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.

Ligand bridging-angle-driven assembly of molecular architectures based on quadruply bonded Mo-Mo dimers

Li, Jian-Rong,Yakovenko, Andrey A.,Lu, Weigang,Timmons, Daren J.,Zhuang, Wenjuan,Yuan, Daqiang,Zhou, Hong-Cai

supporting information; experimental part, p. 17599 - 17610 (2011/02/26)

A systematic exploration of the assembly of Mo2(O 2C-)4-based metal-organic molecular architectures structurally controlled by the bridging angles of rigid organic linkers has been performed. Twelve bridging dicarboxylate ligands were designed to be of different sizes with bridging angles of 0, 60, 90, and 120° while incorporating a variety of nonbridging functional groups, and these ligands were used as linkers. These dicarboxylate linkers assemble with quadruply bonded Mo-Mo clusters acting as nodes to give 13 molecular architectures, termed metal-organic polygons/polyhedra with metal cluster node arrangements of a linear shape, triangle, octahedron, and cuboctahedron/anti-cuboctahedron. The syntheses of these complexes have been optimized and their structures determined by single-crystal X-ray diffraction. The results have shown that the shape and size of the resulting molecular architecture can be controlled by tuning the bridging angle and size of the linker, respectively. Functionalization of the linker can adjust the solubility of the ensuing molecular assembly but has little or no effect on the geometry of the product. Preliminary gas adsorption, spectroscopic, and electrochemical properties of selected members were also studied. The present work is trying to enrich metal-containing supramolecular chemistry through the inclusion of well-characterized quadruply bonded Mo-Mo units into the structures, which can widen the prospect of additional electronic functionality, thereby leading to novel properties.

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