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Journal articles on the topic '2,6-dimethylpiperidine'

Author: Grafiati

Published: 4 June 2021

Last updated: 6 February 2022

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1

Jones, Peter G., Jerzy Ossowski, Piotr Kus, and Ina Dix. "Three Crystal Structures of Terephthalic Acid Salts of Simple Amines." Zeitschrift für Naturforschung B 64, no. 7 (2009): 865–70. http://dx.doi.org/10.1515/znb-2009-0716.

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Diphenethylamine forms two adducts (1 : 1, 1a and 2 : 1, 1b) with terephthalic acid (H2TPA). The former is bis(diphenethylammonium)H2TPA・TPA2− and the latter is bis(diphenethylammonium) ・TPA2−. The amine cis-2,6-dimethylpiperidine forms a hydrated 2 : 1 adduct, bis(2,6-dimethylpiperidinium) ・TPA2−・H2O (2). The crystal structures of all three compounds were determined. All H2TPA and TPA2− residues display inversion symmetry, while the water oxygen atom of 2 lies on a twofold axis. Packing analyses have identified some supramolecular synthons known from related structures.

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2

Mašlejová, Anna, Mária Hvastijová, and Jiří Kohout. "Preparation and Structural Characterization of Cyanatocopper(II) Complexes with Substituted Piperidines." Collection of Czechoslovak Chemical Communications 57, no. 9 (1992): 1899–904. http://dx.doi.org/10.1135/cccc19921899.

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Coordination geometry of the newly prepared complex compounds of [Cu(NCO)2L2] type (L is piperidine, 2-methylpiperidine, 4-methylpiperidine and 2,6-dimethylpiperidine) was investigated at room temperature utilizing the results of infrared, electronic and ESR spectra and magnetic moments. All complexes show a tetragonal arrangement with small axial interaction depending on steric properties of the piperidine ligand given.

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3

Deacon, Glen B., Peter C. Junk, and Jenny Luu. "Nucleophilic Aromatic Substitution of Bis(pentafluorophenyl)mercury with Various Bulky Nucleophiles and the Structures of [Hg(C6F4X-4)2] (X=cyclo-C5H10N, OCH(CH3)2, OC(CH3)3)." Australian Journal of Chemistry 66, no. 10 (2013): 1253. http://dx.doi.org/10.1071/ch13227.

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Reactions of bis(pentafluorophenyl)mercury with piperidine, sodium iso-propoxide or sodium tert-butoxide have yielded the corresponding 4-substituted tetrafluorophenylmercurials, [Hg(C6F4X-4)2] (X = cyclo-C5H10N (1), OCH(CH3)2 (2), OC(CH3)3 (3)), in reasonable yields but the bulkier nucleophiles, cis-2,6-dimethylpiperidine and 2,6-di-iso-propylphenolate (from sodium 2,6-di-iso-propylphenolate) decomposed the mercurial into pentafluorobenzene. Treatment of bis(pentafluorophenyl)mercury with another bulky nucleophile, 2,6-diphenylphenolate (from sodium 2,6-diphenylphenolate), in methanol, result

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4

Ośmiałowski, Borys, Erkki Kolehmainen, Ryszard Gawinecki, Robert Dobosz, and Reijo Kauppinen. "Complexation of 2,6-Bis(acylamino)pyridines with Dipyridin-2-ylamine and 4,4-Dimethylpiperidine-2,6-dione." Journal of Physical Chemistry A 114, no. 49 (2010): 12881–87. http://dx.doi.org/10.1021/jp1084857.

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5

Shou-Ning, CHAI. "Deuterium Isotope Effects on the Critical Behavior of 2,6-Dimethylpiperidine+Water System." Acta Physico-Chimica Sinica 25, no. 05 (2009): 847–52. http://dx.doi.org/10.3866/pku.whxb20090515.

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6

Ballerat-Busserolles, Karine, Mickaël R. Simond, Yohann Coulier, and Jean-Yves Coxam. "Protonation of alkanolamines and cyclic amines in water at temperatures from 293.15 to 373.15 K." Pure and Applied Chemistry 86, no. 2 (2014): 233–43. http://dx.doi.org/10.1515/pac-2014-5017.

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Abstract The protonation properties of amines are of particular interest for the development of thermodynamic models representative of CO2 dissolution in aqueous solutions. This paper reports experimental equilibrium constants of protonation of alkanolamines (2-aminoethanol, 2,2′-iminodiethanol, 2-[bis(2-hydroxyethyl)amino]ethanol, 2-amino-2-methylpropan-1-ol, 2,2′-(methylimino)diethanol and cyclic amines (morpholine, 4-methylmorpholine, pyridine, 1-methyl-piperidine, 2-methyl-piperidine, 2,6-dimethylpiperidine). The equilibrium constants of protonation were determined by potentiometric techni

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7

Kumar, M. Dinesh, P. Rajesh, R. Priya Dharsini, and M. Ezhil Inban. "Molecular Geometry, NLO, MEP, HOMO-LUMO and Mulliken Charges of Substituted Piperidine Phenyl Hydrazines by Using Density Functional Theory." Asian Journal of Chemistry 32, no. 2 (2019): 401–7. http://dx.doi.org/10.14233/ajchem.2020.22444.

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The quantum chemical calculations of organic compounds viz. (E)-1-(2,6-bis(4-chlorophenyl)-3-ethylpiperidine-4-ylidene)-2-phenyl-hydrazine (3ECl), (E)-1-(2,6-bis(4-chlorophenyl)-3-methylpiperidine-4-ylidene)-2-phenylhydrazine (3MCl) and (E)-1-(2,6-bis(4-chloro-phenyl)-3,5-dimethylpiperidine-4-ylidene)-2-phenylhydrazine (3,5-DMCl) have been performed by density functional theory (DFT) using B3LYP method with 6-311G (d,p) basis set. The electronic properties such as Frontier orbital and band gap energies have been calculated using DFT. Global reactivity descriptor has been computed to predict ch

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8

Mori, Atsunori, Shunsuke Tamba, Kenji Ide, Keisuke Shono, and Atsushi Sugie. "Deprotonative Metalation of Chlorothiophene with Grignard Reagents and Catalytic cis-2,6-Dimethylpiperidine under Mild Conditions." Synlett 24, no. 09 (2013): 1133–36. http://dx.doi.org/10.1055/s-0033-1338385.

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9

Ton, Quoc Cuong, and Ernst Egert. "Cocrystals of the antibiotic trimethoprim with glutarimide and 3,3-dimethylglutarimide held together by three hydrogen bonds." Acta Crystallographica Section C Structural Chemistry 71, no. 1 (2015): 75–79. http://dx.doi.org/10.1107/s2053229614027193.

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The antibiotic trimethoprim [5-(3,4,5-trimethoxybenzyl)pyrimidine-2,4-diamine] was cocrystallized with glutarimide (piperidine-2,6-dione) and its 3,3-dimethyl derivative (4,4-dimethylpiperidine-2,6-dione). The cocrystals,viz.trimethoprim–glutarimide (1/1), C14H18N4O3·C5H7NO2, (I), and trimethoprim–3,3-dimethylglutarimide (1/1), C14H18N4O3·C7H11NO2, (II), are held together by three neighbouring hydrogen bonds (one central N—H...N and two N—H...O) between the pyrimidine ring of trimethoprim and the imide group of glutarimide, with anADA/DADpattern (A= acceptor andD= donor). These heterodimers re

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10

Jeon, Soo-Bin, Sang-Won Cho, Sang-Sup Lee, Se-Yong Jang, and Kwang-Joong Oh. "Absorption characteristics of carbon dioxide into an O/W emulsion absorbent containing N-methylcyclohexylamine/2,6-dimethylpiperidine." Journal of the Taiwan Institute of Chemical Engineers 45, no. 5 (2014): 2673–80. http://dx.doi.org/10.1016/j.jtice.2014.08.008.

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11

Xu, Chen, Xue Wang, Zhiyun Chen, Tianxiang Yin, and Weiguo Shen. "Measurements of heat capacities and turbidities for binary mixtures {water + 2,6-dimethylpyridine} and {water, or heavy water + 2,6-dimethylpiperidine} in the critical regions." Fluid Phase Equilibria 409 (February 2016): 361–68. http://dx.doi.org/10.1016/j.fluid.2015.10.027.

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12

Tamba, Shunsuke, Kenji Ide, Keisuke Shono, Atsushi Sugie, and Atsunori Mori. "ChemInform Abstract: Deprotonative Metalation of Chlorothiophene with Grignard Reagents and Catalytic cis-2,6-Dimethylpiperidine under Mild Conditions." ChemInform 44, no. 39 (2013): no. http://dx.doi.org/10.1002/chin.201339102.

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13

Manhas, B. S., M. P. Kaur, K. Kaur, B. C. Verma, and S. B. Kalia. "Synthesis and Studies on Nickel(III) and Copper(III) Complexes of 3-Methyl-, 4-Methyl- And 2,6-Dimethylpiperidine Carbodithioates." Synthesis and Reactivity in Inorganic and Metal-Organic Chemistry 29, no. 6 (1999): 1009–21. http://dx.doi.org/10.1080/00945719909349507.

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14

Jeon, Soo-Bin, Jong-Hyeon Jung, Hyung-Don Lee, Bong-Jun Kim, and Kwang-Joong Oh. "Absorption of carbon dioxide in O/W emulsion absorbent: Kinetics of absorption in N -methylcyclohexylamine and 2,6-dimethylpiperidine emulsion." International Journal of Greenhouse Gas Control 44 (January 2016): 1–10. http://dx.doi.org/10.1016/j.ijggc.2015.11.003.

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15

Mokbel, Ilham, Antonio Razzouk, Terufat Sawaya, and Jacques Jose. "Experimental Vapor Pressures of 2-Phenylethylamine, Benzylamine, Triethylamine, andcis-2,6-Dimethylpiperidine in the Range between 0.2 Pa and 75 kPa." Journal of Chemical & Engineering Data 54, no. 3 (2009): 819–22. http://dx.doi.org/10.1021/je800603z.

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16

Žilionis, Andrius. "Nitrogen-containing cyclic compounds as iminium ion sources for selected reaction monitoring detection of derivatized analytes." European Journal of Mass Spectrometry 26, no. 1 (2019): 25–35. http://dx.doi.org/10.1177/1469066719869817.

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Liquid chromatography–tandem mass spectrometry is one of the most sensitive tools for determination of trace amounts of analytes in metabolomics and proteomics. The highest sensitivity is achieved in selected reaction monitoring detection, which involves fragmentation of the molecular ion between two levels of mass selection. However, fragmentation of some compounds is complicated. Detection sensitivity of such analytes may be increased by derivatizing them with a specific moiety fragmentation of which results in product ion of high abundance. In this work, we reveal the influence of iminium i

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17

Koman, M., E. Ďurčanská, M. Handlovič, and J. Gažo. "Structural investigations of NiII complexes. V. Preparation, properties and structure of bis(2,6-dimethylpiperidine)di(thiocyanato-N)nickel(II)–benzene, [Ni(NCS)2(C7H15N)2].C6H6." Acta Crystallographica Section C Crystal Structure Communications 41, no. 10 (1985): 1418–20. http://dx.doi.org/10.1107/s0108270185008010.

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18

Rana, Abu Safieh, Muhi Eldeen Zuhair, Alsarahni Aseel, and Al-Kaissi Elham. "Synthesis and Structural Elucidation of Aminoacetylenic Derivatives of 7-Methoxy- 2-Naphthole as Antimicrobial Agents." International Journal of Pharmaceutical and Clinical Research 9, no. 08 (2017). http://dx.doi.org/10.25258/ijpcr.v9i08.9589.

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A new series of 7-methoxy-2-[4-(t-amino-1-yl)oxy]-naphthalene derivatives; 7-methoxy-2-{[4-(2-methylpiperidine)but-2-yn-1-yl]oxy}-naphthalene (RZ2), 7-methoxy-2-{[4-(2,6-dimethylpiperidine)but-2-yn-1-yl]oxy}-naphthalene (RZ3), 7-methoxy-2{[4-(piperidine)but-2-yn-1-yl]oxy}-naphthalene (RZ4), 7-methoxy-2-{[4-(pyrrolidine)but-2-yn-1-yl]oxy}-naphthalene (RZ5), 7-methoxy-2-{[4-(N-methylpiperazine)but-2-yn-1-yl]oxy}-naphthalene (RZ6), 7-methoxy -2-{[4-(hexamethyleneimine)but-2-yn-1-yl]oxy}-naphthalene (RZ7) were synthesized and screened in vitro as potential antimicrobial agents. Antimicrobial activ

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