Academic literature on the topic 'Methylthiazole'

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Journal articles on the topic "Methylthiazole"

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Dong, Min, and Liang-Dong Sun. "4-Methylthiazole-5-carbaldehyde." Acta Crystallographica Section E Structure Reports Online 61, no. 8 (2005): o2712—o2713. http://dx.doi.org/10.1107/s1600536805023202.

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Nimbalkar, Seijas, Vazquez-Tato, and Nikalje. "Ultrasound-Assisted One Pot Synthesis of Novel 5-(1-(Substituted phenyl)-4,5-diphenyl-1H-imidazol-2-yl)-4-methylthiazole." Proceedings 9, no. 1 (2018): 63. http://dx.doi.org/10.3390/ecsoc-22-05795.

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This work reports synthesis of ten novel derivatives of 5-(1-(substituted phenyl)-4,5-diphenyl-1H-imidazol-2-yl)-4-methylthiazole 5(a–o). The reaction of benzil, primary aryl amines, 4-methylthiazole-5-carbaldehyde and ammonium acetate was carried out in one pot in the presence of eco-friendly catalyst Ceric ammonium nitrate in solvent ethanol to give final compounds. The structures of the synthesized compounds were confirmed by spectral characterization such as IR, 1H-NMR, 13C-NMR and mass spectral studies.
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Song, Qing Bao, Zhi Min Jin, Hai Bin Wang, and Biao Jiang. "N′-(Benzenesulfonyl)-4-methylthiazole-5-carbohydrazide." Acta Crystallographica Section E Structure Reports Online 60, no. 8 (2004): o1292—o1293. http://dx.doi.org/10.1107/s1600536804015806.

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Abel, M. D., A. D. Cameron, C. M. Ha, et al. "Novel Azolylalkyloxy Compounds with Antipicornaviral Activity." Antiviral Chemistry and Chemotherapy 6, no. 4 (1995): 245–54. http://dx.doi.org/10.1177/095632029500600407.

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A novel series of azolylalkyloxy compounds was designed, synthesized and evaluated for antipicornaviral activity. Several of the compounds exhibited in vitro activity comparable to that of Disoxarll. An investigation of qualitative structure-activity relationships indicated that the optimal length of the alkyI chain is six or seven carbon atoms, with seven being marginally superior. The effect of different azole moieties on activity was relatively small, with 3-methylisoxazole and 4-methylthiazole being most effective. The nature of the oxy substituent was found to be extremely important for a
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Antonov, E. A., A. A. Zhirov, A. T. Kirsanov, et al. "Synthesis of 5-(2-chloroethyl)-4-methylthiazole using the reaction of 5-(2-hydroxyethyl)-4-methylthiazole with phosphorus pentachloride." Pharmaceutical Chemistry Journal 33, no. 12 (1999): 658–60. http://dx.doi.org/10.1007/bf02974943.

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Hartung, Jens, Kristina Daniel, Ingrid Svoboda, and Hartmut Fuess. "5-(4-Methoxyphenyl)-4-methylthiazole-2(3H)-thione." Acta Crystallographica Section E Structure Reports Online 61, no. 6 (2005): o1744—o1746. http://dx.doi.org/10.1107/s1600536805013863.

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Gol'dfarb, Ya L., G. P. Gromova, and L. I. Belen'kii. "Course of bromination of thiazole and 2-methylthiazole." Chemistry of Heterocyclic Compounds 22, no. 6 (1986): 663–66. http://dx.doi.org/10.1007/bf00575251.

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Antonov, E. A., A. A. Zhirov, A. T. Kirsanov, et al. "ChemInform Abstract: Synthesis of 5-(2-Chloroethyl)-4-methylthiazole by Reaction of 5-(2-Hydroxyethyl)-4-methylthiazole with Phosphorus Pentachloride." ChemInform 31, no. 16 (2010): no. http://dx.doi.org/10.1002/chin.200016056.

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Jäger, W., and H. Mäder. "The Microwave Spectrum of 4-Methylthiazole: Methyl Internal Rotation, 14N Nuclear Quadrupole Coupling and Electric Dipole Moment." Zeitschrift für Naturforschung A 42, no. 12 (1987): 1405–9. http://dx.doi.org/10.1515/zna-1987-1208.

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The microwave spectrum of 4-methylthiazole has been investigated in the frequency region from 8 to 36 GHz, employing both Fourier transform and Stark spectroscopy. The results of 14N quadrupole hyperfine structure, methyl internal rotation and fourth order centrifugal distortion analyses are given. The dipole moment components could be determined from the Stark splittings of some rotational lines.
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Yunnikova, L. P., T. A. Akent'eva, and E. A. Yunnikova. "C- or N- functionalization of tropilia salt 2-amino-4-methylthiazole or 5-aminotetrazole." Журнал органической химии 59, no. 11 (2023): 1497–500. http://dx.doi.org/10.31857/s0514749223110125.

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The charges on the reaction centers of 2-amino-4-methylthiazole and 5-aminotetrazole, which predetermine their interaction with tropylium tetrafluoroborate, were determined by quantum chemical calculation (AM1) in accordance with the charge control of the process. New compounds 4-methyl-5-(cyclohepta-11,31,51-trienyl)-2-aminothiazole and 5-( N , N -dicyclohepta-11,31,51-trienyl)aminotetrazole were obtained.
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Dissertations / Theses on the topic "Methylthiazole"

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Nguyen, Thi Thuy. "Structures and internal dynamics of methylated nitrogen containing aromatic rings probed by means of microwave spectroscopy, quantum chemical calculation and spectral modelling." Electronic Thesis or Diss., Université Paris Cité, 2021. http://www.theses.fr/2021UNIP7368.

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Ce travail est dédié à l'étude des signatures de rotation de six cycles aromatiques contenant de l'azote et un ou deux groupes méthyles (2-méthylthiazole (2MTA), 2-méthypyrrole (2MP), 3-méthylpyrrole (3MP), 2,5-diméthylpyrrole (25DMP) 4,5-diméthylthiazole (45DMTA), 4-méthylpyrimidine (4MPY)) - des précurseurs d'hydrocarbures aromatiques polycycliques qui jouent un rôle crucial en astrochimie et ont le potentiel d'être détectés dans l'espace. Notre étude vise à affiner la compréhension des effets de mouvement(s) de grande amplitude du (des) groupe(s) méthyle(s), en produisant des constantes mol
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Book chapters on the topic "Methylthiazole"

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Demaison, J. "430 C4H5NS 2-Methylthiazole." In Asymmetric Top Molecules. Part 2. Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-10400-8_178.

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Conference papers on the topic "Methylthiazole"

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Cummings, Charlotte, and Nick Nguyen, Walker. "BARRIERS TO INTERNAL ROTATION AND MOLECULAR GEOMETRIES OF COMPLEXES FORMED BETWEEN ISOMERS OF METHYLTHIAZOLE AND WATER STUDIED BY MICROWAVE SPECTROSCOPY." In 2023 International Symposium on Molecular Spectroscopy. University of Illinois at Urbana-Champaign, 2023. http://dx.doi.org/10.15278/isms.2023.6915.

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Nimir, Hassan, Norah Al Mohaideb, Mariem Hamad, et al. "Synthesis, Characterization, Crystal Structures, and in vitro Antitumor Activity of Palladium and Platinum (Ii) Complexes with 2-Acetyl-4-Methylthiazole Thiosemicarbazone and 2-Acetylpyrazine Thiosemicarbazone." In Qatar Foundation Annual Research Conference Proceedings. Hamad bin Khalifa University Press (HBKU Press), 2016. http://dx.doi.org/10.5339/qfarc.2016.hbpp3347.

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Akpinar, Ayse Nur, Selvi Secil Sahin, Büşra Moran Bozer, Aziz Tekin, and Cansu Ekin Gumus-Bonacına. "Effect of Food Emulsions on the Cytotoxicity of 3-chloropropane-1,2-diol Esters." In 2022 AOCS Annual Meeting & Expo. American Oil Chemists' Society (AOCS), 2022. http://dx.doi.org/10.21748/emiq3563.

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3-Chloropropane-1,2-diol (3-MCPD) esters are food processing contaminants, and are known to be potentially carcinogenic. The main purpose of this study was to determine whether the emulsion technique increases the absorption of this contaminant, and to develop strategies to reduce their absorption. 3-MCPD ester contents in edible oils (hazelnut, walnut, sunflower, soybean, corn, and olive oil) were determined. Refined olive oil contained the highest 3-MCPD ester level (1.7749 ± 0.1262 mg/kg). Then, emulsions (fine, medium, coarse) were prepared with 0.15-2% emulsifier (whey protein isolate) an
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