Product Name :
2-Pyridinecarboxaldehyde (CAS 1121-60-4)
Synonym :
2-Formylpyridine, Picolinaldehyde
Application :
CAS:
1121-60-4
Purity:
≥99%
Molecular Weight:
107.11
Formula :
C6H5NO
Physical state:
Liquid
solubility :
Shipping Condition :
Store at 4° C
Melting point:
-20.99° C
SMILES:
C1=CC=NC(=C1)C=O
References:
:Complexation to Fe(II), Ni(II), and Zn(II) of multidentate ligands resulting from condensation of 2-pyridinecarboxaldehyde with alpha,omega-triamines: selective imidazolidine/hexahydropyrimidine ring opening revisited. | Bréfuel, N., et al. 2005. Inorg Chem. 44: 8916-28. PMID: 16296847Selective complexation of 3d metal(II) ions with multidentate and chiral isomers derived from condensation of 2-pyridinecarboxaldehyde with triethylenetetramine. | Lee, YM., et al. 2009. Dalton Trans. 126-33. PMID: 19081980Isoreticular metalation of metal-organic frameworks. | Doonan, CJ., et al. 2009. J Am Chem Soc. 131: 9492-3. PMID: 19534523Cyclic Acetal Formation Between 2-Pyridinecarboxaldehyde and gamma-Hydroxy-alpha,beta-Acetylenic Esters.Price of 1885090-83-4 | Osman, S.1370535-33-3 manufacturer and Koide, K.PMID:33673794 2008. Tetrahedron Lett. 49: 6550-6552. PMID: 19907635Metal-Arene Complexes with Indolo[3,2-c]-quinolines: Effects of Ruthenium vs Osmium and Modifications of the Lactam Unit on Intermolecular Interactions, Anticancer Activity, Cell Cycle, and Cellular Accumulation. | Filak, LK., et al. 2013. Organometallics. 32: 903-914. PMID: 23431223Synthesis, characterization, fluorescence and catalytic activity of some new complexes of unsymmetrical Schiff base of 2-pyridinecarboxaldehyde with 2,6-diaminopyridine. | Ali, OA., et al. 2015. Spectrochim Acta A Mol Biomol Spectrosc. 144: 99-106. PMID: 25748987N-terminal specific conjugation of extracellular matrix proteins to 2-pyridinecarboxaldehyde functionalized polyacrylamide hydrogels. | Lee, JP., et al. 2016. Biomaterials. 102: 268-76. PMID: 27348850Novel 2-pyridinecarboxaldehyde thiosemicarbazones Ga(III) complexes with a high antiproliferative activity by promoting apoptosis and inhibiting cell cycle. | Qi, J., et al. 2017. Eur J Med Chem. 134: 34-42. PMID: 28395152Cytosolic Delivery of Proteins Using Amphiphilic Polymers with 2-Pyridinecarboxaldehyde Groups for Site-Selective Attachment. | Sangsuwan, R., et al. 2019. J Am Chem Soc. 141: 2376-2383. PMID: 30663873Memantine-Derived Schiff Bases as Transdermal Prodrug Candidates. | Araujo de Oliveira, AP., et al. 2022. ACS Omega. 7: 11678-11687. PMID: 35449959Single-Step N-Terminal Modification of Proteins via a Bio-Inspired Copper(II)-Mediated Aldol Reaction. | Hanaya, K., et al. 2022. Chemistry. 28: e202201677. PMID: 35723525Sustainable Coordination Polymer-Based Catalyst and Its Application in the Nitroaromatic Hydrogenation under Mild Conditions. | Aghajani, S. and Mohammadikish, M. 2022. Langmuir. 38: 8686-8695. PMID: 35802934PBC, an easy and efficient strategy for high-throughput protein C-terminome profiling. | Zhai, L., et al. 2022. Front Cell Dev Biol. 10: 995590. PMID: 36120566