2,6-Diformylpyridine

2,6-Diformylpyridine.svg 90 Pyridine-2,6-dicarbaldehyde 2,6-Pyridinedialdehyde 5431-44-7 correct FDA FX6E2354Y8 71798 226-589-6 79485 1S/C7H5NO2/c9-4-6-2-1-3-7(5-10)8-6/h1-5H PMWXGSWIOOVHEQ-UHFFFAOYSA-N C1=CC(=NC(=C1)C=O)C=O white solid 124 07 Warning 315 319 335 261 264 271 280 302+352 304+340 305+351+338 312 321 332+313 337+313 362 403+233 405 501 2,6-Diformylpyridine is an organic compound with the formula C5H3N(CHO)2, and typically appears as a solid powder at room temperature. The molecule features formyl groups adjacent to the nitrogen of pyridine. The compound is prepared by oxidation of 2,6-dimethylpyridine.10.1016/S0166-9834(00)82465-3 Vapour Phase Oxidation of 2,6-Lutidine to 2,6-Pyridinedicarboxaldehyde. III: Kinetic Study 1987 Forni Lucio Casalone Gianluigi Applied Catalysis 34 317–328 It condenses with amines to give diiminopyridine ligands,10.1021/ja990449w Iron and Cobalt Ethylene Polymerization Catalysts Bearing 2,6-Bis(Imino)Pyridyl Ligands: Synthesis, Structures, and Polymerization Studies 1999 Britovsek George J. P. Bruce Michael Gibson Vernon C. Kimberley Brian S. Maddox Peter J. Mastroianni Sergio McTavish Stuart J. Redshaw Carl Solan Gregory A. Strömberg Staffan White Andrew J. P. Williams David J. Journal of the American Chemical Society 121 38 8728–8740 as was demonstrated in Fraser Stoddart's synthesis of molecular Borromean rings. 10.1126/science.1096914 Molecular Borromean Rings 2004 Chichak K. S. Cantrill S. J. Pease A. R. Chiu S.-H. Cave G. W. V. Atwood J. L. Stoddart J. F. James Fraser Stoddart Science 304 5675 1308–1312 15166376 2004Sci...304.1308C 45191675 http://irep.ntu.ac.uk/id/eprint/22968/1/196491_534%20Cave%20PostPrint.pdf10.1039/B505730B Nanoscale Borromean links for real 2005 Peters Andrea J. Chichak Kelly S. Cantrill Stuart J. Stoddart J. Fraser James Fraser Stoddart Chemical Communications 27 3394–6 15997275 188 Historical Perspective on the Discovery of Covalent Organic Frameworks https://books.google.com/books?id=06iODwAAQBAJ&pg=PA188 Introduction to Reticular Chemistry: Metal-Organic Frameworks and Covalent Organic Frameworks Omar M. Yaghi Omar M. Yaghi Markus J. Kalmutzki Christian S. Diercks Wiley-VCH 2019 978-3-527-82108-2 It also finds use in the preparation of metal-coordinated polymer materials.10.1002/marc.202200790 Metal Coordination in Polyimine Covalent Adaptable Networks for Tunable Material Properties and Enhanced Creep Resistance Sybren K. Schoustra Maarten M. J. Smulders Macromolecular Rapid Communications 2023 44 5 2200790 36629864 255593988 free 10.1039/C2CC32656F Metallodynameric membranes – toward the constitutional transport of gases G. Nasr T. Macron A. Gilles Z. Mouline M. Barboiu Chemical Communications 2012 48 54 6827–6829 22652555 Related compounds 2,6-Diacetylpyridine Isophthalaldehyde References Category:Aromatic aldehydes Category:Disubstituted pyridines