User:Imareaver/4-pyridylnicotinamide

N-(Pyridin-4-yl)nicotinamide
Names
	IUPAC name N-pyridin-4-ylpyridine-3-carboxamide
	Other names 4-pna; 3-pyridinecarboxamide, N-4-pyridinyl-; 4-Pyridylnicotinamide
Identifiers
CAS Number	64479-79-4;
3D model (JSmol)	Interactive image;
ChemSpider	2311305 ;
	SMILES O=C(Nc1ccncc1)c2cccnc2;
Properties
Chemical formula	C11H9N3O
Molar mass	199.20 g/mol
Density	1.287 g/cm3
Boiling point	286.08°C
Structure
Dipole moment	0 D
Hazards
Flash point	126.817 °C
Related compounds
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). verify (what is ?) Infobox references

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N-(Pyridin-4-yl)nicotinamide (4-pna) is a kinked dipodal dipyridine which was originally developed for use in chemotherapy ^[1] The nitrogen atoms on its pyridine rings can donate their electron lone pairs to metal cations, allowing it to bridge metal centers and act as a bidentate ligand in coordination polymers.^[2]^[3] ^[4] ^[5] It is synthesized through the reaction of nicotinoyl chloride and 4-Aminopyridine.^[1]

References[edit]

^ ^a ^b Gardner, T. S.; Wenis, E.; Lee, J. (1954). "The Synthesis of Compounds for the Chemotherapy of Tuberculosis. Iv. The Amide Function". The Journal of Organic Chemistry. 19 (5): 753. doi:10.1021/jo01370a009.
^ Kraft, P. E.; Laduca, R. L. (2012). "Catena-Poly\\tetra-μ-benzoato-κ8O:O′-dicopper(II)]-μ-\N-(pyridin-4-yl)nicotinamide]-κ2N:N′-\dibenzoato-κ2O-copper(II)]-μ-\N-(pyridin-4-yl)nicotinamide]-κ2N:N′]". Acta Crystallographica Section E Structure Reports Online. 68 (8): m1049. doi:10.1107/S1600536812030437.
^ Krishna Kumar, D. (2009). "Exploring the effect of chain length of bridging ligands in coordination complexes and polymers derived from mixed ligand systems of pyridylnicotinamides and dicarboxylates". Inorganica Chimica Acta. 362 (6): 1767–2013. doi:10.1016/j.ica.2008.08.033.
^ Kumar, D. K.; Das, A.; Dastidar, P. (2006). "One-Dimensional Chains, Two-Dimensional Corrugated Sheets Having a Cross-Linked Helix in Metal−Organic Frameworks: Exploring Hydrogen-Bond Capable Backbones and Ligating Topologies in Mixed Ligand Systems". Crystal Growth & Design. 6 (8): 1903. doi:10.1021/cg0600344.
^ Kumar, D. K.; Das, A.; Dastidar, P. (2006). "Exploring hydrogen-bond capable backbone and ligating topologies: Co(II) coordination polymers derived from mixed ligand systems". Journal of Molecular Structure. 796: 139. doi:10.1016/j.molstruc.2006.02.033.

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[GTS-1] Gardner, T. S.; Wenis, E.; Lee, J. (1954). "The Synthesis of Compounds for the Chemotherapy of Tuberculosis. Iv. The Amide Function". The Journal of Organic Chemistry. 19 (5): 753. doi:10.1021/jo01370a009.

[2] Kraft, P. E.; Laduca, R. L. (2012). "Catena-Poly\\tetra-μ-benzoato-κ8O:O′-dicopper(II)]-μ-\N-(pyridin-4-yl)nicotinamide]-κ2N:N′-\dibenzoato-κ2O-copper(II)]-μ-\N-(pyridin-4-yl)nicotinamide]-κ2N:N′]". Acta Crystallographica Section E Structure Reports Online. 68 (8): m1049. doi:10.1107/S1600536812030437.

[3] Krishna Kumar, D. (2009). "Exploring the effect of chain length of bridging ligands in coordination complexes and polymers derived from mixed ligand systems of pyridylnicotinamides and dicarboxylates". Inorganica Chimica Acta. 362 (6): 1767–2013. doi:10.1016/j.ica.2008.08.033.

[4] Kumar, D. K.; Das, A.; Dastidar, P. (2006). "One-Dimensional Chains, Two-Dimensional Corrugated Sheets Having a Cross-Linked Helix in Metal−Organic Frameworks: Exploring Hydrogen-Bond Capable Backbones and Ligating Topologies in Mixed Ligand Systems". Crystal Growth & Design. 6 (8): 1903. doi:10.1021/cg0600344.

[5] Kumar, D. K.; Das, A.; Dastidar, P. (2006). "Exploring hydrogen-bond capable backbone and ligating topologies: Co(II) coordination polymers derived from mixed ligand systems". Journal of Molecular Structure. 796: 139. doi:10.1016/j.molstruc.2006.02.033.

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