2,6-Dimethylpyridine-4-carbaldehyde

2,6-Dimethylpyridine-4-carbaldehyde

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D13895 Technical Data Sheet

MDL: MFCD06410687

Molecular Formula: C₈H₉NO

CAS Number: 18206-06-9

Storage: Store at 2-8 C^o, under dry conditions.

Synonyms: 2,6-Dimethylisonicotinaldehyde, 18206-06-9, 2,6-dimethylpyridine-4-carbaldehyde, 2,6-Dimethylpyridine-4-carboxaldehyde, 4-formyl-2,6-dimethylpyridine, 2,6-dimethyl-4-pyridinecarboxaldehyde, 4-Pyridinecarboxaldehyde, 2,6-dimethyl-, 4 Pyridinecarboxaldehyde,2,6-dimethyl-

Uses: Synthesis building block, Organic Synthesis, pyridine nitrogen heterocycle, synthesis, aldehyde reactions

2,6-Dimethylpyridine-4-carbaldehyde, is a synthetic fine chemical useful in the synthesis of pharmaceuticals and fine organic chemicals.

Selected References:

1-Substituted 4-Aryl-5-pyridinylimidazoles: A New Class of Cytokine Suppressive Drugs with Low 5-Lipoxygenase and Cyclooxygenase Inhibitory Potency, Boehm, Jeffrey C., Smietana, Juanita M., Sorenson, Margaret E., Garigipati, Ravi S., Gallagher, Timothy F., Sheldrake, Peter L., Bradbeer, Jeremy, Badger, Alison M., Laydon, Jeffrey T., et al., Journal of Medicinal Chemistry (1996), 39(20), 3929-3937. DOI:10.1021/JM960415O

Optical pH Sensor Covering the Range from pH 0-14 Compatible with Mobile-Device Readout and Based on a Set of Rationally Designed Indicator Dyes,  Gotor, Raul, Ashokkumar, Pichandi, Hecht, Mandy, Keil, Karin, Rurack, Knut, Analytical Chemistry (Washington, DC, United States) (2017), 89(16), 8437-8444., DOI:10.1021/acs.analchem.7b01903

Synthesis and pH-sensitive luminescence of bis-terpyridyl iridium(III) complexes incorporating pendent pyridyl groups, Arm, Kathryn J., Leslie, Wendy, Williams, J. A. Gareth, Inorganica Chimica Acta (2006), 359(4), 1222-1232. DOI:10.1016/j.ica.2005.09.021

Selective photosensitization through an AND logic response: optimization of the pH and glutathione response of activatable photosensitizers, Erbas-Cakmak, Sundus, Cakmak, Fatma Pir, Topel, Seda Demirel, Uyar, Taha Bilal, Akkaya, Engin U.,  Chemical Communications (Cambridge, United Kingdom) (2015), 51(61), 12258-12261. DOI:10.1039/C5CC01261A

https://www.ncbi.nlm.nih.gov/pubmed/26134889

Preparation of azolylmethylaminotetrahydroquinolines and related compounds as chemokine receptor binding agents.,  Bridger, Gary, Skerlj, Renato, Kaller, Al, Harwig, Curtis, Bogucki, David, Wilson, Trevor R., Crawford, Jason, McEachern, Ernest J., Atsma, Bem, Nan, Siqiao, et al, PCT Int. Appl. (2002), WO 2002022600 A2 20020321

Preparation of substituted pyrazolo[1,5-a]pyridine compounds as RET kinase inhibitors, Andrews, Steven W., Aronow, Sean, Blake, James F., Brandhuber, Barbara J., Cook, Adam, Haas, Julia, Jiang, Yutong, Kolakowski, Gabrielle R., McFaddin, Elizabeth A., McKenney, Megan L., et al, PCT Int. Appl. (2018), WO 2018071447 A1 20180419

Preparation and antibacterial activity of tricyclic carbapenem compounds,  Rossi, Tino, Andreotti, Daniele, Tedesco, Giovanna, Tarsi, Luca, Ratti, Emiliangelo, Feriani, Aldo, Pizzi, Domenica Antonia, Gaviraghi, Giovari, Biondi, Stefano, Finizia, Gabriella, PCT Int. Appl. (1998), WO 9821210 A1 19980522,

Preparation of substituted 2-phenyl-3H-quinazolin-4-ones and analogs as antiinflammatory and cardiovascular agents, Hansen, C. Henrik,  PCT Int. Appl. (2010), WO 2010106436 A2 20100923

Derivatives of 2,4,6-collidine and 2,4-lutidine, Mathes, Wilhelm, Sauermilch, Walter, Chemische Berichte (1955), 88, 1276-83.

Preparation of substituted diazaspirononanes as OGA inhibitors, Bartolome-Nebreda, Jose Manuel, Trabanco-Suarez, Andres Avelino, Martinez Viturro, Carlos Manuel, PCT Int. Appl. (2018), WO 2018141984 A1 20180809