Relevant bibliographies by topics / Dimethylpyridine

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Dimethylpyridine'

Author: Grafiati
Published: 5 June 2025
Last updated: 1 August 2025

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Journal articles on the topic "Dimethylpyridine"

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Igor, A. Parshikov, I. Zaraisky Evgeny, and M. Khasaeva Fatima. "Degradation of 2,6-dimethylpyridine by Arthrobacter crystallopoietes." Ecology, Environment and Conservation 22, no. 4 (2017): 1673–76. https://doi.org/10.5281/zenodo.1157087.

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Degradation of pyridines in waste water is an important issue for chemical and pharmaceutical industries. The biodegradation of 2,6-dimethylpyridine was investigated by the bacterium Arthrobacter crystallopoietes KM-4, which resulted in the formation of three metabolites: 2,6-dimethylpyridin-3-ol, 2,6-dimethylpyridin-3,4-diol, and 2,4-dioxopentanoic acid.
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Šilhánková, Alexandra, Jana Hulvová, Petr Trška, and Miloslav Ferles. "Condensation reactions of 2,4- and 2,6-dimethylpyridines and their 1-oxides." Collection of Czechoslovak Chemical Communications 54, no. 6 (1989): 1687–704. http://dx.doi.org/10.1135/cccc19891687.

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Using the reactions of 2,4- and 2,6-dimethylpyridine-1-oxides with aromatic and heteroaromatic aldehydes under catalysis with potassium tert-butoxide (E)-aryl- and (E)-heteroarylethenylpyridine-1-oxides IIIa-IIIe, IVa-IVc, Va, Vb respectively, were prepared. 1-Oxides IIIg, IVd, IVe and Vc were obtained from the appropriate pyridine bases by oxidation with peracetic acid. Condensation of 2,4- and 2,6-dimethylpyridines with 3-pyridinecarbaldehyde gives a mixture of bases VIa and VIc, and VIb and VId, respectively. On Claisen condensation of 2,6- or 2,4-dimethylpyridine-1-oxide with diethyl oxala
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Amrollahi, Mohammad Ali. "Synthesis of Fluorinated Pyridines as 19F NMR pH Indicators." JOURNAL OF ADVANCES IN CHEMISTRY 10, no. 3 (2014): 2441–46. http://dx.doi.org/10.24297/jac.v10i3.2275.

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This research was undertaken to synthesizes and evaluate 3,5-dihydroxymethyl-4-(2-fluorophenyl)-2,6-dimethylpyridine and 4-(fluoromethyl)-2,6-dimethylpyridine as indicators of 19F NMR pH. A comparison of 3,5-dihydroxymethyl-4-(2-fluorophenyl)-2,6-dimethylpyridine to 4-(fluoromethyl)-2,6-dimethylpyridine showed that 4-(fluoromethyl)-2,6-dimethylpyridine has a large 19F chemical shift to pH, a suitable pKa value and a good water solubility.
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Hensena, Karl, Markus Kettner, Thorsten Stumpf, and Michael Bolte. "Synthese und Kristallstrukturbestimmung von Silicium-Komplexen der Koordinationszahl sechs mit Dimethylpyridinen/ Syntheses and Crystal Structure Determination of Hexacoordinated Silicon-Complexes with Dimethylpyridines." Zeitschrift für Naturforschung B 55, no. 10 (2000): 901–6. http://dx.doi.org/10.1515/znb-2000-1003.

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Abstract Trichlorosilane, HSiCl3, forms with 3,4-dimethylpyridine in aprotic solvents a crystalline l:2-compound which is stable at room temperature and readily soluble in CHCl3. Colourless crystals of the dicationic complex, [H2Si(3,4-dimethylpyridine)4]2+ 2Cl- · 6 CHCl3 (verified by X-ray structure analysis) are obtained by dismutation of HSiCl3(3,4-dimethylpyridine)2 in CHCl3 within one week at room temperature.29Si NM R indicates that SiCl4 is generated as a second product. H2SiCl2 with 2,4-dimethylpyridine as well as MeHSiBr2 with 3,5-dimethylpyridine in aprotic solvents form 1:2-compound
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Döring, Cindy, and Peter G. Jones. "Crystal structures of seven gold(III) complexes of the form LAuX 3 (L = substituted pyridine, X = Cl or Br)." Acta Crystallographica Section E Crystallographic Communications 80, no. 8 (2024): 894–909. http://dx.doi.org/10.1107/s2056989024007266.

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The structures of seven gold(III) halide derivatives of general formula LAuX 3 (L = methylpyridines or dimethylpyridines, X = Cl or Br) are presented: trichlorido(2-methylpyridine)gold(III), [AuCl3(C6H7N)], 1 (as two polymorphs 1a and 1b); tribromido(2-methylpyridine)gold(III), [AuBr3(C6H7N)], 2; tribromido(3-methylpyridine)gold(III), [AuBr3(C6H7N)], 3; tribromido(2,4-dimethylpyridine)gold(III), [AuBr3(C7H9N)], 4; trichlorido(3,5-dimethylpyridine)gold(III), [AuCl3(C7H9N)], 5; tribromido(3,5-dimethylpyridine)gold(III), [AuBr3(C7H9N)], 6, and trichlorido(2,6-dimethylpyridine)gold(III), [AuCl3(C7
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Pugh, David. "2,6-Dibromo-3,5-dimethylpyridine and 2,6-diiodo-3,5-dimethylpyridine." Acta Crystallographica Section C Crystal Structure Communications 62, no. 10 (2006): o590—o592. http://dx.doi.org/10.1107/s0108270106032732.

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Vasetska, Olesia P., Mykola G. Prodanchuk, and Petro G. Zhminko. "ANTIHYPOXIC ACTIVITY OF 2,6-DIMETHYLPYRIDINE-N-OXIDE." Wiadomości Lekarskie 75, no. 12 (2022): 2974–81. http://dx.doi.org/10.36740/wlek202212114.

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The aim: To study the antihypoxic activity of 2,6-dimethylpyridine-N-oxide in mice using the various experimental models of acute hypoxia under orally or intraperitoneally administration. Materials and methods: The studies were performed on male CD-1 (SPF) mice. The antihypoxic activity of 2,6-dimethylpyridine-N-oxide was studied in three experimental models of acute hypoxia - hypercapnic hypoxia or hypoxia in a closed space, hemic hypoxia and histotoxic hypoxia at orally administration at doses 0.07; 7.1 and 71 mg/kg (respectively 1/20000, 1/200 and 1/20 of LD50) and at intraperitoneally admi
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Wibaut, J. P., and E. C. Kooyman. "Syntheses of 3,4-dimethylpyridine, 2,3-dimethylpyridine and 2-methyl-3-ethylpyridine." Recueil des Travaux Chimiques des Pays-Bas 63, no. 12 (2010): 231–38. http://dx.doi.org/10.1002/recl.19440631202.

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Suckert, Stefan, Inke Jess та Christian Näther. "Crystal structure of bis(3,5-dimethylpyridine-κN)bis(methanol-κO)bis(thiocyanato-κN)cobalt(II)". Acta Crystallographica Section E Crystallographic Communications 72, № 12 (2016): 1824–26. http://dx.doi.org/10.1107/s2056989016018326.

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The asymmetric unit of the title complex, [Co(NCS)2(C7H9N)2(CH3OH)2], comprises of one CoIIcation located on a centre of inversion, one thiocyanate ligand, one methanol ligand and one 3,5-dimethylpyridine ligand. The CoIIcation is octahedrally coordinated by two terminal N-bonding thiocyanate anions, two methanol molecules and two 3,5-dimethylpyridine ligands into a discrete complex. The complex molecules are linked by intermolecular O—H...S hydrogen bonding into chains that elongate in the direction parallel to thebaxis.
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Hensen, Karl, Alexander Lemke, and Michael Bolte. "Lewis-Säure/Base Addukte von TiCl4 und Methylpyridinen / Lewis Acid/Base Adducts of TiCl4 and Methylpyridines." Zeitschrift für Naturforschung B 55, no. 9 (2000): 877–81. http://dx.doi.org/10.1515/znb-2000-0912.

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By the reaction of 2-methyl- and 2,6-dimethylpyridine the first neutral TiCl4L complexes (L = single bonded ligand) could be synthesized. The structures have been determined by single crystal X-ray methods. The best description of the molecular structure is a distorted trigonal bipyramid with the nitrogen base occupying an equatorial position. With 2,4-dimethylpyridine, a 1:2 adduct is formed, where the nitrogen bases are in trans-positions of a TiCl4N2-octahedron, as also confirmed by an X-ray analysis
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Dissertations / Theses on the topic "Dimethylpyridine"

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ABDALA, VALENCIA HIAM. "Implication des phospholipases a2 de leishmania dans l'invasion et la survie : cible potentielle de derives de la 2-amino-4,6-dimethylpyridine." Nantes, 2001. http://www.theses.fr/2001NANT06VS.

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Liao, Yu-an, and 廖御安. "Synthesis of functionalized tetraindole analogs with a central 2,5-dimethylpyridine core structure." Thesis, 2011. http://ndltd.ncl.edu.tw/handle/07531794611328002886.

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碩士<br>國立中正大學<br>化學暨生物化學研究所<br>99<br>Utilization of indole substructure as the pharmacophore has been recognized as an important strategy to design antitumor agents for biomedical applications. Toward developing antitumor agents, our research group contributed by designing various indole analogues, which possess different numbers of indole moiety, a free N atom, and various electron-donating substitutes on indole ring and show promising effects in different cancer cell lines. In comparison to its indole counterpart tetraindole, SK228, with a central core structure of benzene exhibits a high pot
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Books on the topic "Dimethylpyridine"

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Jungk, Manfred. Statische und dynamische Streulichtmessungen am System 2,6-Dimethylpyridin/Wasser in der Nähe des unteren kritischen Entmischungspunktes. [s.n.], 1986.

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Book chapters on the topic "Dimethylpyridine"

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Wohlfarth, Christian. "Viscosity of 2,6-dimethylpyridine." In Viscosity of Pure Organic Liquids and Binary Liquid Mixtures. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-49218-5_256.

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Wohlfarth, Ch. "Dielectric constant of 2,6-dimethylpyridine." In Supplement to IV/6. Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-75506-7_231.

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Wohlfarth, Ch. "Surface tension of 2,6-dimethylpyridine." In Supplement to IV/16. Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-75508-1_139.

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Wohlfarth, Christian. "Refractive index of 2,6-dimethylpyridine." In Optical Constants. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-49236-9_280.

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Wohlfarth, Ch. "Dielectric constant of the mixture (1) acetonitrile; (2) 2,6-dimethylpyridine." In Supplement to IV/6. Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-75506-7_505.

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Wohlfarth, Ch. "Surface tension of the mixture (1) water; (2) 2,6-dimethylpyridine." In Supplement to IV/16. Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-75508-1_252.

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Wohlfarth, Christian. "Refractive index of binary liquid mixture of water and 2,6-dimethylpyridine." In Optical Constants. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-49236-9_437.

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Wohlfarth, Christian. "Viscosity of the binary liquid mixture of water and 2,6-dimethylpyridine." In Viscosity of Pure Organic Liquids and Binary Liquid Mixtures. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-49218-5_514.

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Wohlfarth, Christian. "Viscosity of the binary liquid mixture of methanol and 2,6-dimethylpyridine." In Viscosity of Pure Organic Liquids and Binary Liquid Mixtures. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-49218-5_610.

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Cibulka, I., L. Hnědkovský, J. C. Fontaine, K. Sosnkowska-Kehiaian, and H. V. Kehiaian. "Volumetric Properties of the Mixture Hexane C6H14 + C7H9N 2,4-Dimethylpyridine (LB2233, VMSD1211)." In Binary Liquid Systems of Nonelectrolytes. Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-73584-7_2748.

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Conference papers on the topic "Dimethylpyridine"

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Cheng, Jing, Chaojie Zhang, and Qi Zhou. "Study on Influence Factors of Nitrogenous Heterocyclic Compound-Dimethylpyridine Degradation under Anoxic Conditions." In 2009 3rd International Conference on Bioinformatics and Biomedical Engineering (iCBBE). IEEE, 2009. http://dx.doi.org/10.1109/icbbe.2009.5163479.

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Singh, Kuldeep, Preeti Verma, and Rajni Kant. "X-ray structure analysis of bis(O-amyldithiocarbonato)bis(3,5-dimethylpyridine)nickel(II)." In 3RD INTERNATIONAL CONFERENCE ON CONDENSED MATTER AND APPLIED PHYSICS (ICC-2019). AIP Publishing, 2020. http://dx.doi.org/10.1063/5.0002033.

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Maki, Hiroaki, Koichiro Sadakane, Takahiro Kenmotsu, Naomichi Ito, and Kenichi Yoshikawa. "The viscosity of the mixture of water / 2,6-dimethylpyridine / NaBPh4 at lamellar phase and disordered phase." In 2015 International Symposium on Micro-NanoMechatronics and Human Science (MHS). IEEE, 2015. http://dx.doi.org/10.1109/mhs.2015.7438249.

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Reports on the topic "Dimethylpyridine"

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Khasaeva, Fatima, Igor Parshikov, and Evgeny Zaraisky. Degradation of 2,6-dimethylpyridine by Arthrobacter crystallopoietes. Intellectual Archive, 2020. http://dx.doi.org/10.32370/iaj.2463.

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Degradation of pyridines in waste water is an important issue for chemical and pharmaceutical industries. The biodegradation of 2,6-dimethylpyridine was investigated by the bacterium Arthrobacter crystallopoietes KM-4, which resulted in the formation of three metabolites: 2,6-dimethylpyridin-3-ol, 2,6-dimethylpyridin- 3,4-diol, and 2,4-dioxopentanoic acid.
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