Relevant bibliographies by topics / Methylpyrazol

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  1. Journal articles
  2. Dissertations / Theses
  3. Book chapters
  4. Conference papers

Academic literature on the topic 'Methylpyrazol'

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

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Journal articles on the topic "Methylpyrazol"

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Sirianni, Eric R., Glenn P. A. Yap, Eser S. Akturk, and Klaus H. Theopold. "Improved syntheses, and structural and electronic characterization of carboxamide-substituted TpCONHPh,Meand TpCONHt-Bu,Meligands." Acta Crystallographica Section C Crystal Structure Communications 69, no. 9 (2013): 947–53. http://dx.doi.org/10.1107/s0108270113015898.

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Improvements in the syntheses of the carboxamide-substituted tris(pyrazolyl)borate ligands TpCONHPh,Me[tris(3-anilinocarbonyl-5-methylpyrazol-1-yl)borate] and TpCONHt-Bu,Me[tris(3-tert-butylaminocarbonyl-5-methylpyrazol-1-yl)borate] are reported. Their TlIsalts, namely [tris(3-anilinocarbonyl-5-methylpyrazol-1-yl-κN2)borato]thallium(I), [Tl(C33H31BN9O3)], (II), and [tris(3-tert-butylaminocarbonyl-5-methylpyrazol-1-yl-κN2)borato]thallium(I), [Tl(C27H43BN9O3)], (III), as well as the CuIcarbonyl complexes (TpCONHPh,Me)Cu(CO), namely carbonyl[tris(3-anilinocarbonyl-5-methylpyrazol-1-yl-κN2)borato]
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Perrin, Monique, Alain Thozet, Pilar Cabildo, Rosa Ma Claramunt, Eduard Valenti, and José Elguero. "Molecular structure and tautomerism of 3,5-bis(4-methylpyrazol-1-yl)-4-methylpyrazole." Canadian Journal of Chemistry 71, no. 9 (1993): 1443–49. http://dx.doi.org/10.1139/v93-186.

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The title compound C12N6H14, 1, crystallizes in the space group P21/n (a = 8.222(2) Å, b = 27.336(8) Å, c = 5.574(2) Å, α = 90.00°, β = 100.97(4)°, γ = 90.00°), Z = 4, d = 1.308 g cm−3. The conformation about the N—C bonds linking the pyrazole rings can be defined as EZ, with "pyridine-like" nitrogen atoms in an anti disposition [Formula: see text] and "pyridine-like" and "pyrrole-like" nitrogen atoms in a syn disposition [Formula: see text] with regard to the central pyrazole. Intermolecular hydrogen bonds between the central and the terminal pyrazole ring of configuration Z form centrosymmet
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Fedotov, S. O., and A. S. Hotsulia. "Synthesis and properties of 3-(ethylthio)-9-methyl-6-(alkylthio)pyrazolo[1,5-d][1,2,4]triazolo[3,4-f][1,2,4]triazines." Current issues in pharmacy and medicine: science and practice 15, no. 3 (2022): 227–34. http://dx.doi.org/10.14739/2409-2932.2022.3.263994.

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The combination of pyrazole and 1,2,4-triazole fragments in one structure makes it possible to achieve some success in creating potential biologically active compounds. Various factors contribute to this process. Among them, we can note the significant possibilities of chemical transformation involving these cycles, the simplicity, and reliability of methods, the creation of molecules with a certain level of bioavailability and the ability to influence a number of biochemical processes. Taking into account the presented facts, the creation of new compounds in a number of pyrazolo-triazole cond
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Claramunt, R. M., C. Lopez, D. Sanz, et al. "Rhodium(I) complexes with the polydentate ligand 3,5-bis(4-methylpyrazol-1-yl)-4-methylpyrazole." Journal of Organometallic Chemistry 412, no. 1-2 (1991): 259–71. http://dx.doi.org/10.1016/0022-328x(91)86061-t.

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Díaz, José Luis, Jordi Corbera, Daniel Martínez, et al. "Pyrazolo[3,4-d]pyrimidines as sigma-1 receptor ligands for the treatment of pain. Part 2: Introduction of cyclic substituents in position 4." MedChemComm 8, no. 6 (2017): 1246–54. http://dx.doi.org/10.1039/c7md00078b.

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R., HARODE, and C. SHARMA T. "Synthesis of 2-(3'-Methylpyrazol-5-one-l'-yl)-4-arylthiazoles." Journal of Indian Chemical Society Vol. 66, Apr 1989 (1989): 282–83. https://doi.org/10.5281/zenodo.6140328.

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School of Studies in Chemistry, Vikram University, Ujjain-456 010 <em>Manuscript received 8 June 1988,&nbsp; accepted 2 February 1989</em> Synthesis of 2-(3&#39;-Methylpyrazol-5-one-I&#39;-yl)-4-arylthiazoles
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Dial, Sharon M., Mary Anna Hull Thrall, and Dwayne W. Hamar. "Comparison of ethanol and 4-methylpyrazole as treatments for ethylene glycol intoxication in cats." American Journal of Veterinary Research 55, no. 12 (1994): 1771–82. http://dx.doi.org/10.2460/ajvr.1994.55.12.1771.

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Summary The efficacy of 4-methylpyrazole (4-mp) and ethanol as treatment for ethylene glycol (eg) intoxication in cats was compared. Twenty-two cats were assigned at random to 6 experimental groups. Cats of 1 experimental group were given only 4-mp; those of another experimental group were given only eg. Cats of 3 experimental groups were intoxicated with eg and given 4-mp at 0 hour or 2 or 3 hours after eg ingestion, and those of 1 experimental group were given eg and treated with ethanol 3 hours after eg ingestion. Physical, biochemical, hematologic, blood gas, serum and urine eg concentrati
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Fedotov, S. O., A. S. Hotsulia, and Yu V. Karpenko. "Synthesis and analgesic activity of new pyrazole-containing derivatives of 1,2,4-triazole-3-thiol." Current issues in pharmacy and medicine: science and practice 16, no. 3 (2023): 205–12. http://dx.doi.org/10.14739/2409-2932.2023.3.288364.

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Pain represents a primary symptom of numerous diseases and conditions, affecting millions of people worldwide. Effective analgesic medications can alleviate or eliminate pain, thereby enhancing patients’ quality of life and assisting them in resuming normal physical and social activities. However, several existing analgesics may carry unwanted side effects, such as ulcers, blood clotting issues, drowsiness, and more. The development of new analgesics is focused on creating drugs that are both effective and associated with fewer adverse effects. Considering the continuous rise in the number of
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Shi, Yao-Cheng, Bei-Bei Zhu, and Seik Weng Ng. "[1-(2-Hydroxyethyl)-5-methylpyrazol-3-yl]ferrocenium chloride and [1-(2-hydroxyethyl)-5-methylpyrazol-3-yl]ferrocene cocrystal." Acta Crystallographica Section E Structure Reports Online 63, no. 5 (2007): m1385—m1387. http://dx.doi.org/10.1107/s160053680701687x.

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Fedotov, S. O., and A. S. Hotsulia. "Synthesis and properties of S-derivatives of 4-amino-5-(5-methylpyrazol-3-yl)-1,2,4-triazole-3-thiol." Current issues in pharmacy and medicine: science and practice 14, no. 3 (2021): 268–74. http://dx.doi.org/10.14739/2409-2932.2021.3.243176.

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The combination of various heterocyclic systems with a wide range of properties is quite expedient and is, in practice, a justified direction for obtaining biologically active substances, which ultimately forms a favorable basis for the creation of drugs. In recent decades, the attention of scientists has been closely focused on nitrogen-containing heterocyclic compounds. Among such compounds, 1,2,4-triazole and pyrazole occupy a special place. Indeed, on the basis of these systems, a significant number of well-known drugs have been created, which are widely used at the present time. The aim o
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Dissertations / Theses on the topic "Methylpyrazol"

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Berta, Holló. "Sinteza i karakterizacija nekih derivata pirazola i njihove reakcije sa prelaznim metalima." Phd thesis, Univerzitet u Novom Sadu, Prirodno-matematički fakultet u Novom Sadu, 2011. http://dx.doi.org/10.2298/NS20110922HOLLO.

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Reactions of 3,5-dimethylpyrazole-1-carboxamidinium&nbsp;nitrate (dpca∙HNO3) and 4-acetyl-3-amino-5-methylpyrazole (aamp) with transition metals under different reaction conditions are presented. The template reaction of aamp with triethyl orthoformate (teof) in the presence of metal ion is described. Besides, condensation of aamp with thiosemicarbazide (tsc) and the coordination of its product to copper(II) ion is also described. Twelve new complex compounds are synthesized and fully characterized. The characterization of two other, already known complexes is significantly enriched. The influ
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Lambert, Catherine. "Tolérance du 4-méthylpyrazole utilisé comme antidote lors des intoxications par l'éthylène-glycol et le méthanol." Paris 5, 1992. http://www.theses.fr/1992PA05P149.

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Chi, Yu-Chou, and 紀毓周. "Oxidation of methanol, ethylene glycol, and isopropanol with human alcohol dehydrogenases and the inhibition by ethanol and 4-methylpyrazole." Thesis, 2011. http://ndltd.ncl.edu.tw/handle/87872468784435081473.

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碩士<br>國防醫學院<br>生物化學研究所<br>99<br>Human alcohol dehydrogenases (ADHs) include multiple isozymes with broad substrate specificity and ethnic distinct allozymes. ADH catalyzes the rate-limiting step in metabolism of various primary and secondary aliphatic alcohols. The oxidation of common toxic alcohols, that is, methanol, ethylene glycol, and isopropanol by the human ADHs remains poorly understood. Kinetic studies were performed in 0.1 M sodium phosphate buffer, at pH 7.5 and 25◦C, containing 0.5 mM NAD+ and varied concentrations of substrate. Km values for ethanol with recombinant human class I A
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Book chapters on the topic "Methylpyrazol"

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of mixed ligand nickel(II) complex with hydrotris(3-phenyl-5-methylpyrazol-1-yl)borate, 3-phenyl-5-methylpyrazole and sodium benzoate." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 8. Springer Berlin Heidelberg, 2023. http://dx.doi.org/10.1007/978-3-662-66460-5_244.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of mixed ligand nickel(II) complex with hydrotris(3-phenyl-5-methylpyrazol-1-yl)borate, 3-phenyl-5-methylpyrazole and sodium p-flourobenzoate." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 8. Springer Berlin Heidelberg, 2023. http://dx.doi.org/10.1007/978-3-662-66460-5_245.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of mixed ligand nickel(II) complex with hydrotris(3-phenyl-5-methylpyrazol-1-yl)borate, 3-phenyl-5-methylpyrazole and sodium p-nitrobenzoate." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 8. Springer Berlin Heidelberg, 2023. http://dx.doi.org/10.1007/978-3-662-66460-5_246.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of dinuclear copper(II) complex with 1, 1′-(4-methylpyrazol-3, 5-diyl)diacetaldehyde dioxime." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-53974-3_363.

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Bährle-Rapp, Marina. "4,5-Diamino-1-Methylpyrazole HCl." In Springer Lexikon Kosmetik und Körperpflege. Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_2837.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of binuclear copper(II) complex of substituted methylpyrazole." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-49202-4_141.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of polymeric cobalt(II) complex of 3-methylpyrazole." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-662-45972-0_487.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of chloro-bridged binuclear copper(II) complex with 5-aminomethyl-3-methylpyrazole." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 4. Springer Berlin Heidelberg, 2021. http://dx.doi.org/10.1007/978-3-662-62474-6_213.

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Stadlbauer, W. "From 3-Methylpyrazoles and α-Oxo Ketenes." In Five-Membered Hetarenes with Two Nitrogen or Phosphorus Atoms. Georg Thieme Verlag KG, 2002. http://dx.doi.org/10.1055/sos-sd-012-00329.

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Conference papers on the topic "Methylpyrazol"

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Babayan, E., R. Ohanian, A. Martirosian, and V. Kaphian. "1. Experimental Evaluation of Toxicity of 3(5) Methylpyrazol (MP)." In AIHce 1998. AIHA, 1999. http://dx.doi.org/10.3320/1.2762586.

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