1309982-39-5 Usage
Uses
Used in Organic Chemistry:
6-(1,3-Dioxolan-2-yl)pyridine-3-boronic acid pinacol ester is used as a building block for the synthesis of various pharmaceuticals and agrochemicals, leveraging its stability and reactivity to form carbon-carbon bonds through cross-coupling reactions.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 6-(1,3-Dioxolan-2-yl)pyridine-3-boronic acid pinacol ester is utilized for the development of novel therapeutic agents, capitalizing on its ability to contribute to the synthesis of complex organic molecules with potential medicinal properties.
Used in Materials Science:
6-(1,3-Dioxolan-2-yl)pyridine-3-boronic acid pinacol ester is employed in materials science for the creation of advanced materials, taking advantage of its chemical properties to enhance the performance and functionality of these materials.
Used in Pharmaceutical Industry:
6-(1,3-Dioxolan-2-yl)pyridine-3-boronic acid pinacol ester is used as a key intermediate in the pharmaceutical industry for the production of various drugs, due to its role in facilitating the synthesis of complex organic molecules with therapeutic potential.
Used in Agrochemical Industry:
In the agrochemical industry, 6-(1,3-Dioxolan-2-yl)pyridine-3-boronic acid pinacol ester is utilized as a precursor in the synthesis of agrochemicals, such as pesticides and herbicides, owing to its ability to form stable and reactive carbon-carbon bonds.
Check Digit Verification of cas no
The CAS Registry Mumber 1309982-39-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,0,9,9,8 and 2 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1309982-39:
(9*1)+(8*3)+(7*0)+(6*9)+(5*9)+(4*8)+(3*2)+(2*3)+(1*9)=185
185 % 10 = 5
So 1309982-39-5 is a valid CAS Registry Number.
1309982-39-5Relevant articles and documents
Luminescent Tetrahedral Molecular Cages Containing Ruthenium(II) Chromophores
Luis, Ena T.,Iranmanesh, Hasti,Arachchige, Kasun S. A.,Donald, William A.,Quach, Gina,Moore, Evan G.,Beves, Jonathon E.
, p. 8476 - 8486 (2018)
We have designed linear metalloligands which contain a central photoactive [Ru(N∞N)3]2+ unit bordered by peripheral metal binding sites. The combination of these metalloligands with Zn(II) and Fe(II) ions leads to heterometallic tetrahedral cages, which were studied by NMR spectroscopy, mass spectrometry, and photophysical methods. Like the parent metalloligands, the cages remain emissive in solution. This approach allows direct incorporation of the favorable properties of ruthenium(II) polypyridyl complexes into larger self-assembled structures.
Meta-Selective C-H Borylation of Benzamides and Pyridines by an Iridium-Lewis Acid Bifunctional Catalyst
Yang, Lichen,Uemura, Nao,Nakao, Yoshiaki
supporting information, p. 7972 - 7979 (2019/05/22)
We report herein the iridium-catalyzed meta-selective C-H borylation of benzamides by using a newly designed 2,2′-bipyridine (bpy) ligand bearing an alkylaluminum biphenoxide moiety. We also demonstrate the iridium-catalyzed C3-selective C-H borylation of pyridine with a 1,10-phenanthroline (Phen) ligand bearing an alkylborane moiety. It is proposed that the Lewis acid-base interaction between the Lewis acid moiety and the aminocarbonyl group or the sp2-hybridized nitrogen atom accelerates the reaction and controls the site-selectivity.
