Relevant bibliographies by topics / Phenylhydrazono

Contents

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

Academic literature on the topic 'Phenylhydrazono'

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

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Journal articles on the topic "Phenylhydrazono"

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P., Venkata Ramana, and K. Ravindranath L. "Synthesis of N' -(2-hydroxybenzoyl)-3-methyl-4-(substitutedphenylhydrazono )-2-pyrazolin-5-ones." Journal of Indian Chemical Society Vol. 76, Feb 1999 (2022): 112–13. https://doi.org/10.5281/zenodo.5852557.

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Department of Chemistry, Sri Krishnadevaraya University, Anantapur-515 003, India <em>Manuscript received 4 February 1998, revised 5 June 1998, accepted 19 August 1998</em> <em>N&#39;</em>-(2-Hydroxybenzoyl)-3-methyl-4-(substituted-phenylhydrazono)-2-pyrazolin-5-ones have been synthesised by the reaction of 2-(substituted-phenylhydrazono)-ethyl-2,3-dioxobutyrate with salicylic acid hydrazine.
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Issac, Yvette A., and Aly A. Aly. "A Convenient Synthesis of New Pentaazacyclopentanaphthalene and Pentaazaphenanthrene Derivates." Zeitschrift für Naturforschung B 58, no. 12 (2003): 1227–33. http://dx.doi.org/10.1515/znb-2003-1212.

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Reaction of N-{3-cyano-6-[4(5-oxo-2-phenylhydrazono-4,5-dihydroimidazol-1-yl)phenyl]-4-phenylpyridin- 2-yl}formimidic ethyl ester (3) and 3-[4-(3-amino-4-imino-5-phenyl-3,4-dihydropyrido[ 2,3-d]pyrimidin-7-yl)phenyl]-2-phenyl-5-phenylhydrazono-3,5-dihydroimidazol-4-one (4) with different reagents has been investigated and discussed. Some of the obtained compounds were tested for their antimicrobial activity.
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El-Ablack, Fawzia Zakaria. "Synthesis of Some New Benzimidazole Derivatives of Pharmaceutical Interest." E-Journal of Chemistry 8, no. 2 (2011): 748–52. http://dx.doi.org/10.1155/2011/723421.

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Reaction of 2-(aminomethyl)benzimidazole dihydrochloride (1) with ethyl acetoacetate was studied to give diazepinone-benzimidazole derivative (2), while, treatment of 1 with phenylhydrazono ethylacetoacetate afforded phenylhydrazino diazepinone derivative (3). On the other hand, reaction of 1 with acetyl acetone resulted in the formation of diazepine derivative (4). The reaction of 1 with ethyl cyanoacetate was studied to give 3-aminodiazepinone derivative (5). Also the reaction of 1 with acetophenone and/or benzophenone has been investigated to give the fused imidazolines 6 and 7 respectively
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Bouchama, Abdelaziz, Abderrahmen Bendaâs, Sofiane Bouacida, Messaoud Yahiaoui, Patricia Benard-Rocherulle, and Amel Djedouani. "(Z)-1,2-Diphenyl-2-(phenylhydrazono)ethanone." Acta Crystallographica Section E Structure Reports Online 63, no. 4 (2007): o1990—o1992. http://dx.doi.org/10.1107/s1600536807012901.

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Gayathri, D., D. Velmurugan, K. Ravikumar, D. Saravanakumar, and M. Kandaswamy. "4-Nitro-2-[(phenylhydrazono)methyl]phenol." Acta Crystallographica Section E Structure Reports Online 63, no. 5 (2007): o2224—o2225. http://dx.doi.org/10.1107/s1600536807015486.

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Rani, Asha, Ajay Prakash Saha, and Satya Murti Prasad. "3-Oxo-2-(phenylhydrazono)butanoic acid." Acta Crystallographica Section E Structure Reports Online 58, no. 9 (2002): o1001—o1002. http://dx.doi.org/10.1107/s1600536802014757.

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Carvalho, Carlos Eduardo M., Antonio V. Pinto та William T. A. Harrison. "3-Bromo-6-phenylhydrazono-β-lapachone". Acta Crystallographica Section E Structure Reports Online 63, № 12 (2007): o4504. http://dx.doi.org/10.1107/s1600536807053810.

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Moustafa, Moustafa Sherief, Saleh Mohammed Al-Mousawi, and Mohamed Hilmy Elnagdi. "Use of a novel multicomponent reaction under high pressure for the efficient construction of a new pyridazino[5,4,3-de][1,6]naphthyridine tricyclic system." RSC Advances 6, no. 93 (2016): 90840–45. http://dx.doi.org/10.1039/c6ra19535k.

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A novel multicomponent reaction between the 2-phenylhydrazono derivative1a, malononitrile and aromatic aldehydes or acetone, carried out under high pressure, was found to generate pyridazino[5,4,3-de][1,6]naphthyridine derivatives9a–hand22.
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D., D. AGARWAL, and AGARWAL VINITA. "Hydrolysis of 2-Phenylhydrazono-1-phenylamlnobutan-1,3-dione." Journal of Indian Chemical Society Vol. 68, Jun 1991 (1991): 360–62. https://doi.org/10.5281/zenodo.6157814.

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School of Studies in Chemistry, Jiwaji University,Gwalior-474 011 <em>Manuscript received 7 November 1990. revised 31 May 1991, accepted&nbsp;31 May 1991</em> Hydrolysis of 2-Phenylhydrazono-1-phenylamlnobutan-1,3-dione.
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Tsolomitis, A., and C. Sandris. "Formation of 3-phenylhydrazono-3-aroylpropionamides from the reaction of 5-aroyl-3(2H)-isothiazolones with phenylhydrazine." Journal of Heterocyclic Chemistry 22, no. 5 (1985): 1465–67. http://dx.doi.org/10.1002/jhet.5570220568.

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Dissertations / Theses on the topic "Phenylhydrazono"

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Puntel, Gustavo Orione. "Análise das propriedades antioxidantes das oximas 3-(fenil hidrazona) butano-2-ona e butano-2,3-dionatiosemicarbazona." Universidade Federal de Santa Maria, 2008. http://repositorio.ufsm.br/handle/1/11087.

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Coordenação de Aperfeiçoamento de Pessoal de Nível Superior<br>Oximes are chemical compounds used to reactivate the inhibited acetylcholinesterase (AChE) enzyme by organophosphates (OPs). The OPs, besides classically recognized as AChE irreversible inhibitors, are also involved in the generation of oxidative stress conditions. However, researches focusing on the possible antioxidant properties of oximes are lacking in the literature. The aim of this study was to investigate the potential antioxidant and toxic properties of 3-(phenylhydrazono)butan-2-one oxime and butane-2,3-dionethiosemicarbaz
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Bombard, Sophie. "Mécanisme d'action de la lipoxygènase-1 de soja : étude à l'aide de phénylhydrazones." Paris 5, 1990. http://www.theses.fr/1990PA05P604.

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Lupo, Donald, Werner Prass, Ude Scheunemann, André Laschewsky, Helmut Ringsdorf, and Isabelle Ledoux. "Second-harmonic generation in Langmuir-Blodgett monolayers of stilbazium salt and phenylhydrazone dyes." Universität Potsdam, 1988. http://opus.kobv.de/ubp/volltexte/2009/1740/.

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Contents: 1. INTRODUCTION 2. SYNTHESIS OF THE COMPOUNDS 3. PREPARATION AND CHARACTERIZATION OF MONOLAYERS A. Monolayer Isotherms B. Langmuir-Blodgett Monolayer Films 4. EXPERIMENTAL SETUP FOR NONLINEAR MEASUREMENTS 5. NONLINEAR OPTICAL PROPERTIES 6. DISCUSSION 7. CONCLUSION
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Alshabanah, Othman A. "Polyamine and acetylpolyamine levels during phenylhydrazine-induced erythropoiesis in mouse spleen." Scholarly Commons, 1988. https://scholarlycommons.pacific.edu/uop_etds/3406.

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The phenylhydrazine-induced erythropoietic mouse spleen is used as a model system to demonstrate the relationship between tissue growth and polyamine metabolism. Phenylhydrazine produced significant changes in spleen weights, hematocrits and reticulocyte counts in Swiss-Webster mice. The average spleen weight went up from a control of 155 mg to 875 mg at 96 hours after phenylhydrazine administration, while a 49% reduction in the value of hematocrit was observed at 72 hours. Reticulocyte counts in peripheral blood went from 0.8 to 58% at 168 hours after treatment with phenylhydrazine. Phenylhyd
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Іншина, Наталія Миколаївна, Наталия Николаевна Иншина, Nataliia Mykolaivna Inshyna та Я. А. Гриценко. "Роль біосинтезу гему в регуляції вмісту цитохрому р-450 за умов фенілгідразинової анемії". Thesis, Сумський державний університет, 2017. http://essuir.sumdu.edu.ua/handle/123456789/55073.

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Як відомо, фенілгідразін є класичним гемолітичним агентом. Метаболізм фенілгідразину здійснюється в печінці за участю цитохрома Р-450 (цх Р-450). В гепатоцитах 70 % гему, синтезованого de novo, використовується для утворення цх Р-450. Регуляторним ферментом біосинтезу гему є 5-амінолевулінатсинтаза (5-АЛК-синтаза).
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Marsella, Adam Manuele. "A new method for the measurement of airborne formaldehyde using derivatization with 3,5-bis(trifluoromethyl)phenylhydrazine." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1999. http://www.collectionscanada.ca/obj/s4/f2/dsk1/tape7/PQDD_0019/MQ45914.pdf.

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Hoang, Jane Vu. "Inactivation of Choline Oxidase by Irreversible Inhibitors or Storage Conditions." Digital Archive @ GSU, 2006. http://digitalarchive.gsu.edu/chemistry_theses/4.

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Choline oxidase from Arthrobacter globiformis is a flavin-dependent enzyme that catalyzes the oxidation of choline to betaine aldehyde through two sequential hydride-transfer steps. The study of this enzyme is of importance to the understanding of glycine betaine biosynthesis found in pathogenic bacterial or economic relevant crop plants as a response to temperature and salt stress in adverse environment. In this study, chemical modification of choline oxidase using two irreversible inhibitors, tetranitromethane and phenylhydrazine, was performed in order to gain insights into the active sit
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EL, HAMDAOUI AZEDDINE. "Degradation du caoutchouc par oxydation controlee. Action du couple phenylhydrazine/oxygene sur des cetones modeles des extremites de chaine." Le Mans, 1991. http://www.theses.fr/1991LEMA1011.

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L'objectif du travail realise est l'identification des extremites de chaine obtenues apres degradation controlee du caoutchouc naturel en phase latex sous l'action du couple phenylhydrazine/oxygene. Le but de la these est de verifier l'hypothese anterieure de transformation des extremites methyl- et phenylcetone en extremites phenylhydrazone puis -(phenylazo)hydroperoxyde par utilisation de molecules modeles de ces extremites fonctionnelles. Le chapitre bibliographique permet d'une part, de mettre en evidence les apports du travail presente par rapport aux connaissances anterieures, et d'autre
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CHALLIOUI, GILLET CAROLE. "Degradation du caoutchouc naturel en phase latex par oxydation controlee. Action du couple phenylhydrazine/oxygene sur un modele des structures polyisopreniques." Le Mans, 1994. http://www.theses.fr/1994LEMA1024.

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Ce memoire traite de l'etude de la degradation controlee du caoutchouc naturel en phase latex sous l'action du couple redox phenylhydrazine/oxygene. En se basant sur les resultats des travaux anterieurs et possedant a present, des methodes d'analyses plus performantes (rmn #1h 400mhz et cg/sm), notre travail a consiste a identifier de maniere plus sure et plus complete les fonctions d'extremites de chaine apres degradation. Pour cela, nous avons cherche dans un premier temps a alimenter notre reflexion en completant nos connaissances des processus d'oxydation et de degradation du polyisoprene
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GASPARD, SARRA. "Chimie de coordination et topologie du site actif de la prostaglandine h synthetase : reactions avec les hydrazines monosubstituees et avec les phenylhydrazones et caracterisation par spectroscopie de resonance raman." Paris 11, 1994. http://www.theses.fr/1994PA112084.

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La prostaglandine h synthetase (pghs) est une hemoproteine qui intervient dans la biosynthese de mediateurs de l'inflammation, les prostaglandines. Les hydrazines monosubstituees rhnnh#2 sont oxydees par la pghs en diazene rn=nh avec formation de la pghsfe(ii) et du complexe pghsfe#i#i-diazene. L'oxydation de ce complexe conduit a un nouveau complexe a liaison fe-c de l'enzyme: pghsfe#i#i#i-r. La formation de ces complexes montre que la pghs possede un site actif ouvert. Les phenylhydrazones constituent une nouvelle classe de substrats suicide de la fonction dioxygenase de la pghs. Les -azohyd
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Books on the topic "Phenylhydrazono"

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R, Cary, Dobson S, Brooke I, et al., eds. Phenylhydrazine. World Health Organization, 2000.

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I, Brooke, and Great Britain. Health and Safety Executive., eds. Phenylhydrazine: Risk assessment document EH72/1. HSE Books, 1997.

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Marsella, Adam Manuele. A new method for the measurement of airborne formaldehyde using derivatization with 3,5-bis(trifluoromethyl)phenylhydrazine. National Library of Canada, 1999.

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Phenylhydrazine. World Health Organization, 2000.

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executive, Health and safety. Phenylhydrazine. Health and Safety Executive (HSE), 1997.

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Mashregi, Mariam. Accelerated cytotoxic mechanism screening of isoniazid and phenylhydrazine using an in vitro hepatocyte inflammation model. 2006.

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Book chapters on the topic "Phenylhydrazono"

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Holze, Rudolf. "Ionic conductivities of phenylhydrazine." In Electrochemistry. Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-662-49251-2_226.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of nickel(II) complex with benzoin phenylhydrazone." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54234-7_201.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of copper(II) complex with benzoin phenylhydrazone." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54237-8_182.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of copper(II) complex of tetraaldehyde phenylhydrazone." 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_248.

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Lattová, Erika, and Hélène Perreault. "Method for Investigation of Oligosaccharides Using Phenylhydrazine Derivatization." In Glycomics. Humana Press, 2008. http://dx.doi.org/10.1007/978-1-59745-022-5_5.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of cobalt(II) chloro complex with benzoin phenylhydrazone." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54231-6_495.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of cobalt(II) nitrato complex with benzoin phenylhydrazone." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54231-6_496.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of nickel(II) thiocyanato complex with benzoin phenylhydrazone." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54234-7_200.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of copper(II) chloro complex with benzoin phenylhydrazone." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54237-8_179.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of copper(II) nitrato complex with benzoin phenylhydrazone." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54237-8_180.

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Conference papers on the topic "Phenylhydrazono"

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Azev, Yu A., O. S. Koptyaeva, O. S. Eltsov, Yu A. Yakovleva, T. A. Pospelova, and V. A. Bakulev. "Benzaldehyde phenylhydrazones as c-nucleophiles for functionalization of quinoxaline-2-one. Unusual transformations of indole-3-carbaldehyde phenylhydrazones." In PROCEEDINGS OF INTERNATIONAL CONFERENCE ON RECENT TRENDS IN MECHANICAL AND MATERIALS ENGINEERING: ICRTMME 2019. AIP Publishing, 2020. http://dx.doi.org/10.1063/5.0018799.

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Hou, Zhanjia, Liying Liu, Lei Xu, et al. "Improved optical nonlinearity of poled phenylhydrazone-doped polymer films." In Photonics China '98, edited by Chuangtian Chen. SPIE, 1998. http://dx.doi.org/10.1117/12.318226.

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Ormachea, Carla, and Cristián A. Ferretti. "In Silico Evaluation of Antioxidant Properties of Cinnamaldehyde Phenylhydrazone." In ECSOC-25. MDPI, 2021. http://dx.doi.org/10.3390/ecsoc-25-11711.

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Franconetti, Antonio, Manuel Gómez-Guillén, Pastora Borrachero, and Francisca Cabrera-Escribano. "Structural studies of phenylhydrazine integration in carbohydrate derivatives." In The 15th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2011. http://dx.doi.org/10.3390/ecsoc-15-00693.

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Atanasković, Ana, Thomas Eichhorn, Dejan Milenković, Dušan Dimić, Goran Kaluđerović, and Jasmina Dimitrić Marković. "Synthesis, spectroscopic, and theoretical analysis of Ru(II)-phenylhydrazine complex." In 2nd International Conference on Chemo and Bioinformatics. Institute for Information Technologies, University of Kragujevac, 2023. http://dx.doi.org/10.46793/iccbi23.395a.

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In recent decades, metal-based chemotherapeutics have attracted considerable attention and excitement within the oncology research community, with ruthenium(II) complexes emerging as a particularly promising class of anticancer agents. In this study, the synthesis of a new ruthenium complex was performed, followed by its structural characterization using NMR and IC spectroscopy. The compound’s infrared spectrum reveals characteristic bands corresponding to N-H and C-H stretching vibrations from sp2 and sp3 hybridized carbon atoms, vibrations of aromatic rings and additional vibrations related
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Sudheesh, P., and K. Chandrasekharan. "Metal Nanoparticle Induced Enhancement in Third-Order Optical Nonlinearity of Phenylhydrazone/PMMA thin films." In International Conference on Fibre Optics and Photonics. OSA, 2012. http://dx.doi.org/10.1364/photonics.2012.tpo.43.

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Soubhye, Jalal. "Dual Anti-Inflammatory and Anti-Bacterial Effects of Phenylhydrazide and Phenylhydrazone Derivatives." In 3rd International Electronic Conference on Medicinal Chemistry. MDPI, 2017. http://dx.doi.org/10.3390/ecmc-3-04699.

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Sudheesh, P., D. Mallikharjuna Rao, and K. Chandrasekharan. "Study on metal nanoparticles induced third-order optical nonlinearity in phenylhydrazone derivatives with DFWM technique." In OPTOELECTRONIC MATERIALS AND THIN FILMS: OMTAT 2013. AIP Publishing LLC, 2014. http://dx.doi.org/10.1063/1.4862002.

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Fauzi’ah, Lina, and Tutik Dwi Wahyuningsih. "Cyclization reaction of 4-nitro-3’-4’-dimethoxychalcone and phenylhydrazine as antibacterial candidate." In 2ND INTERNATIONAL CONFERENCE ON CHEMISTRY, CHEMICAL PROCESS AND ENGINEERING (IC3PE). Author(s), 2018. http://dx.doi.org/10.1063/1.5065021.

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Bako, Rabiu, Abdullahi Yunusa Idris, Asma’u Nasiru Hamza, Gbonjubola O. Adeshina, and Musa Abdullahi Garba. "Synthesis, Characterization, and In-Silico Studies of Some Novel Phenylhydrazone Derivatives as Potential Agents for Antimicrobial Activities." In International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2024. https://doi.org/10.3390/ecsoc-28-20254.

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Reports on the topic "Phenylhydrazono"

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NIOSH skin notation (SK) profiles: phenylhydrazine [CAS No. 100-63-0]. U.S. Department of Health and Human Services, Public Health Service, Centers for Disease Control and Prevention, National Institute for Occupational Safety and Health, 2014. http://dx.doi.org/10.26616/nioshpub2014147.

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