Solubility of 5-(4-methylphenyl)-2-furanpropanoic acid in different organic solvents

Simple item page
dc.citation.epage7
dc.citation.issue7
dc.citation.journalTitleХімія, технологія речовин та їх застосування
dc.citation.spage1
dc.citation.volume1
dc.contributor.affiliationНаціональний університет “Львівська політехніка”
dc.contributor.affiliationЛьвівський національний університет ім. І. Франка
dc.contributor.affiliationІнститут проблем матеріалознавства ім. І. М. Францевича НАНУ
dc.contributor.affiliationLviv Polytechnic National University
dc.contributor.affiliationIvan Franko National University of Lviv
dc.contributor.affiliationFrantsevich Institute for Problems of Materials Science NASU
dc.contributor.authorОгородник, М. Я.
dc.contributor.authorГорак, Ю. І.
dc.contributor.authorОбушак, М. Д.
dc.contributor.authorТищенко, Н. І.
dc.contributor.authorСобечко, І. Б.
dc.contributor.authorOhorodnik, M. Ya.
dc.contributor.authorHorak, Yu. I.
dc.contributor.authorObushak, M. D.
dc.contributor.authorTischenko, N. I.
dc.contributor.authorSobechko, I. B.
dc.coverage.placenameЛьвів
dc.coverage.placenameLviv
dc.date.accessioned2025-09-12T07:59:39Z
dc.date.created2024-02-27
dc.date.issued2024-02-27
dc.description.abstractПід час дослідження оцінено температурні залежності розчинності 5-(4-метилфеніл)-2-фуран пропанової кислоти у різних розчинниках: метил- та етилацетаті, ацетонітрилі, пропан-1-олі та пропан-2-олі. Результати аналізу подано у вигляді лінійних рівнянь за моделлю Шредера, що дало змогу визначити ентальпії, ентропії та енергії Гіббса розчинності за температури 298 К. Теплоти плавлення кислоти визначено за допомогою методу диференційно-термічного аналізу, що дало можливість розрахувати ентальпії, ентропії та енергії Гіббса змішування.
dc.description.abstractIn this study, the temperature dependences of the solubility of 5-(4-methylphenyl)-2 furanpropanoic acid in various solvents were evaluated: methyl and ethyl acetate, acetonitrile, propane-1-ol, and propan-2-ol. The results of the analysis are presented in the form of linear equations according to the Schröder model, which allowed us to determine the enthalpies, entropies, and Gibbs energies of solubility at a temperature of 298.15 K. The melting points of the acid were determined using the method of differential thermal analysis, which allowed us to calculate the enthalpies, entropies, and Gibbs energies of mixing.
dc.format.extent1-7
dc.format.pages7
dc.identifier.citationSolubility of 5-(4-methylphenyl)-2-furanpropanoic acid in different organic solvents / M. Ya. Ohorodnik, Yu. I. Horak, M. D. Obushak, N. I. Tischenko, I. B. Sobechko // Chemistry, Technology and Application of Substances. — Lviv : Lviv Politechnic Publishing House, 2024. — Vol 1. — No 7. — P. 1–7.
dc.identifier.citationenSolubility of 5-(4-methylphenyl)-2-furanpropanoic acid in different organic solvents / M. Ya. Ohorodnik, Yu. I. Horak, M. D. Obushak, N. I. Tischenko, I. B. Sobechko // Chemistry, Technology and Application of Substances. — Lviv : Lviv Politechnic Publishing House, 2024. — Vol 1. — No 7. — P. 1–7.
dc.identifier.doidoi.org/10.23939/ctas2024.01.001
dc.identifier.urihttps://ena.lpnu.ua/handle/ntb/111727
dc.language.isoen
dc.publisherВидавництво Львівської політехніки
dc.publisherLviv Politechnic Publishing House
dc.relation.ispartofХімія, технологія речовин та їх застосування, 7 (1), 2024
dc.relation.ispartofChemistry, Technology and Application of Substances, 7 (1), 2024
dc.relation.references1. Koca, M., Servi, S., Kirilmis, C., Ahmedzade, M., Kazaz, C., Özbek, B., & Ötük, G. (2005). Synthesis and antimicrobial activity of some novel derivatives of ben- zofuran: Part 1. synthesis and antimicrobial activity of (ben- zofuran-2-yl)(3-phenyl-3-methylcyclobutyl) ketoxime derivatives. European Journal of Medicinal Chemistry, 40(12), 1351-1358. https://doi.org/10.1016/j.ejmech.2005.07.004
dc.relation.references2. Kirilmis, C., Ahmedzade, M., Servi, S., Koca, M., Kizirgil, A., & Kazaz, C. (2008). Synthesis and anti- microbial activity of some novel derivatives of benzofuran: Part 2. the synthesis and antimicrobial activity of some novel 1-(1-benzofuran-2-yl)-2-mesitylethanone derivatives. European Journal of Medicinal Chemistry, 43(2), 300-308. https://doi.org/10.1016/j.ejmech.2007.03.023
dc.relation.references3. Chand, K., Rajeshwari, Hiremathad, A., Singh, M., Santos, M. A., & Keri, R. S. (2017). A review on anti- oxidant potential of bioactive heterocycle benzofuran: Natural and synthetic derivatives. Pharmacological Reports, 69(2), 281-295. https://doi.org/10.1016/j.pharep.2016.11.007
dc.relation.references4. Sidwell, R. W., Bailey, K. W., Wong, M.-H., Barnard, D. L., & Smee, D. F. (2005). In vitro and in vivo influenza virus-inhibitory effects of viramidine. Antiviral Research, 68(1), 10-17. https://doi.org/10.1016/j.antiviral.2005.06.003
dc.relation.references5. Wang, M., Cao, R., Zhang, L., Yang, X., Liu, J., Xu, M., Shi, Z., Hu, Z., Zhong, W., & Xiao, G. (2020). Remdesivir and chloroquine effectively inhibit the recently emerged novel coronavirus (2019-ncov) in vitro. Cell Research, 30(3), 269-271. https://doi.org/10.1038/s41422-020-0282-0
dc.relation.references6. Rahimzadeh N., Alizadeh M., Ghaemmaghami Hezaveh S. J. Estimated bioaccessibility to 5-hydroxy- methylfurfural from frequently consumed dried fruits in Iran. J Chem Health Risks. 2018;4(3). DOI: 10.22034/jchr. 2018.544071
dc.relation.references7. Yan, F., Wang, A., & Jia, Z. (2004). Benzofuran derivatives from ligularia stenocephala. Journal of the Chinese Chemical Society, 51(4), 863-868. https://doi.org/10.1002/jccs.200400130
dc.relation.references8. Klachko, O., Matiychuk, V., Sobechko, I., Serheyev, V., & Tishchenko, N. (2020). Thermodynamic properties of 6-methyl-2-oxo-4-aryl-1,2,3,4-tetrahydropy- rimidine-5-carboxylic acid esters. Chemistry & Che- mical Technology, 14(3), 277-283. https://doi.org/10.23939/chcht14.03.277
dc.relation.references9. Sobechko, I., Dibrivnyi, V., Horak, Y., Velychkivska, N., Kochubei, V., & Obushak, M. (2017). Thermodynamic properties of solubility of 2-methyl-5- arylfuran-3-carboxylic acids in organic solvents. Chemistry & Chemical Technology, 11(4), 397-404. https://doi.org/10.23939/chcht11.04.397
dc.relation.references10. Sobechko, I., Horak, Y., Dibrivnyi, V., Obushak, M., & Goshko, L. (2019). Thermodynamic properties of 2- methyl-5-arylfuran-3 carboxylic acids chlorine derivatives in organic solvents. Chemistry & Chemical Technology, 13(3), 280-287. https://doi.org/10.23939/chcht13.03.280
dc.relation.references11. Voloshynets' V. A., Reshetnyak O. V. (2014). Nats. un-t "L'viv. politekhnika". L'viv: Vyd-vo L'viv. politekhniky. 155 s. : mal. Bibliohr.: s. 139.
dc.relation.references12. Kos R. V., Sobechko І. B., Kochubey V. V., Vahula A. R., Sergeev V. V. (2016). Solubility of ethyl ester of 2-cyano-3-[5-(4-methylphenyl)-2-furan] acrylic acid in organic solvents. Bulletin of Lviv Polytechnic National University: Chemistry, technology of substances and their application, 841, 14-20. https://doi.org/10.22606/mocr.2017.22006
dc.relation.references13. Ridka, O., Matiychuk, V., Sobechko, I., Ty- shchenko, N., Novyk, M., Sergeev, V., & Goshko, L. (2019). Thermodynamic properties of methyl 4-(4-methoxyphenyl)- 6-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate in Organic Solutions. French-Ukrainian Journal of Chemistry, 7(2), 1-8. https://doi.org/10.17721/fujcv7i2p1-8
dc.relation.references14. Sobechko I., Prokop R., Kochubey V., Melnyk G., Horak Y. Thermodynamics of solutions of 5-phenyl-2- methyl-3-furancarboxylic acid in organic solvents (2014) Lviv University Bulletin. Chemical Series, 55(2), 372-379.
dc.relation.referencesen1. Koca, M., Servi, S., Kirilmis, C., Ahmedzade, M., Kazaz, C., Özbek, B., & Ötük, G. (2005). Synthesis and antimicrobial activity of some novel derivatives of ben- zofuran: Part 1. synthesis and antimicrobial activity of (ben- zofuran-2-yl)(3-phenyl-3-methylcyclobutyl) ketoxime derivatives. European Journal of Medicinal Chemistry, 40(12), 1351-1358. https://doi.org/10.1016/j.ejmech.2005.07.004
dc.relation.referencesen2. Kirilmis, C., Ahmedzade, M., Servi, S., Koca, M., Kizirgil, A., & Kazaz, C. (2008). Synthesis and anti- microbial activity of some novel derivatives of benzofuran: Part 2. the synthesis and antimicrobial activity of some novel 1-(1-benzofuran-2-yl)-2-mesitylethanone derivatives. European Journal of Medicinal Chemistry, 43(2), 300-308. https://doi.org/10.1016/j.ejmech.2007.03.023
dc.relation.referencesen3. Chand, K., Rajeshwari, Hiremathad, A., Singh, M., Santos, M. A., & Keri, R. S. (2017). A review on anti- oxidant potential of bioactive heterocycle benzofuran: Natural and synthetic derivatives. Pharmacological Reports, 69(2), 281-295. https://doi.org/10.1016/j.pharep.2016.11.007
dc.relation.referencesen4. Sidwell, R. W., Bailey, K. W., Wong, M.-H., Barnard, D. L., & Smee, D. F. (2005). In vitro and in vivo influenza virus-inhibitory effects of viramidine. Antiviral Research, 68(1), 10-17. https://doi.org/10.1016/j.antiviral.2005.06.003
dc.relation.referencesen5. Wang, M., Cao, R., Zhang, L., Yang, X., Liu, J., Xu, M., Shi, Z., Hu, Z., Zhong, W., & Xiao, G. (2020). Remdesivir and chloroquine effectively inhibit the recently emerged novel coronavirus (2019-ncov) in vitro. Cell Research, 30(3), 269-271. https://doi.org/10.1038/s41422-020-0282-0
dc.relation.referencesen6. Rahimzadeh N., Alizadeh M., Ghaemmaghami Hezaveh S. J. Estimated bioaccessibility to 5-hydroxy- methylfurfural from frequently consumed dried fruits in Iran. J Chem Health Risks. 2018;4(3). DOI: 10.22034/jchr. 2018.544071
dc.relation.referencesen7. Yan, F., Wang, A., & Jia, Z. (2004). Benzofuran derivatives from ligularia stenocephala. Journal of the Chinese Chemical Society, 51(4), 863-868. https://doi.org/10.1002/jccs.200400130
dc.relation.referencesen8. Klachko, O., Matiychuk, V., Sobechko, I., Serheyev, V., & Tishchenko, N. (2020). Thermodynamic properties of 6-methyl-2-oxo-4-aryl-1,2,3,4-tetrahydropy- rimidine-5-carboxylic acid esters. Chemistry & Che- mical Technology, 14(3), 277-283. https://doi.org/10.23939/chcht14.03.277
dc.relation.referencesen9. Sobechko, I., Dibrivnyi, V., Horak, Y., Velychkivska, N., Kochubei, V., & Obushak, M. (2017). Thermodynamic properties of solubility of 2-methyl-5- arylfuran-3-carboxylic acids in organic solvents. Chemistry & Chemical Technology, 11(4), 397-404. https://doi.org/10.23939/chcht11.04.397
dc.relation.referencesen10. Sobechko, I., Horak, Y., Dibrivnyi, V., Obushak, M., & Goshko, L. (2019). Thermodynamic properties of 2- methyl-5-arylfuran-3 carboxylic acids chlorine derivatives in organic solvents. Chemistry & Chemical Technology, 13(3), 280-287. https://doi.org/10.23939/chcht13.03.280
dc.relation.referencesen11. Voloshynets' V. A., Reshetnyak O. V. (2014). Nats. un-t "L'viv. politekhnika". L'viv: Vyd-vo L'viv. politekhniky. 155 s. : mal. Bibliohr., s. 139.
dc.relation.referencesen12. Kos R. V., Sobechko I. B., Kochubey V. V., Vahula A. R., Sergeev V. V. (2016). Solubility of ethyl ester of 2-cyano-3-[5-(4-methylphenyl)-2-furan] acrylic acid in organic solvents. Bulletin of Lviv Polytechnic National University: Chemistry, technology of substances and their application, 841, 14-20. https://doi.org/10.22606/mocr.2017.22006
dc.relation.referencesen13. Ridka, O., Matiychuk, V., Sobechko, I., Ty- shchenko, N., Novyk, M., Sergeev, V., & Goshko, L. (2019). Thermodynamic properties of methyl 4-(4-methoxyphenyl)- 6-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate in Organic Solutions. French-Ukrainian Journal of Chemistry, 7(2), 1-8. https://doi.org/10.17721/fujcv7i2p1-8
dc.relation.referencesen14. Sobechko I., Prokop R., Kochubey V., Melnyk G., Horak Y. Thermodynamics of solutions of 5-phenyl-2- methyl-3-furancarboxylic acid in organic solvents (2014) Lviv University Bulletin. Chemical Series, 55(2), 372-379.
dc.relation.urihttps://doi.org/10.1016/j.ejmech.2005.07.004
dc.relation.urihttps://doi.org/10.1016/j.ejmech.2007.03.023
dc.relation.urihttps://doi.org/10.1016/j.pharep.2016.11.007
dc.relation.urihttps://doi.org/10.1016/j.antiviral.2005.06.003
dc.relation.urihttps://doi.org/10.1038/s41422-020-0282-0
dc.relation.urihttps://doi.org/10.1002/jccs.200400130
dc.relation.urihttps://doi.org/10.23939/chcht14.03.277
dc.relation.urihttps://doi.org/10.23939/chcht11.04.397
dc.relation.urihttps://doi.org/10.23939/chcht13.03.280
dc.relation.urihttps://doi.org/10.22606/mocr.2017.22006
dc.relation.urihttps://doi.org/10.17721/fujcv7i2p1-8
dc.rights.holder© Національний університет “Львівська політехніка”, 2024
dc.subjectрозчинність
dc.subjectентальпія розчинення
dc.subjectентальпія змішування
dc.subjectентальпія плавлення
dc.subject5-(4-метилфеніл)-2-фуранпропанова кислота
dc.subjectsolubility
dc.subjectenthalpy of dissolution
dc.subjectenthalpy of mixing
dc.subjectenthalpy of fusion
dc.subject5-(4-methylphenyl)-2-furanpropanoic acid
dc.titleSolubility of 5-(4-methylphenyl)-2-furanpropanoic acid in different organic solvents
dc.title.alternativeРозчинність 5-(4-метилфеніл)-2-фуранпропанової кислоти в різних органічних розчинниках
dc.typeArticle

Files

Original bundle

Now showing 1 - 2 of 2
Thumbnail Image
Name:
2024v1n7_Ohorodnik_M_Ya-Solubility_of_5_4_methylphenyl_1-7.pdf
Size:
565.83 KB
Format:
Adobe Portable Document Format
Download
Thumbnail Image
Name:
2024v1n7_Ohorodnik_M_Ya-Solubility_of_5_4_methylphenyl_1-7__COVER.png
Size:
457.68 KB
Format:
Portable Network Graphics
Download

License bundle

Now showing 1 - 1 of 1
Thumbnail Image
Name:
license.txt
Size:
1.92 KB
Format:
Plain Text
Description:
Download

Collections

Chemistry, Technology and Application of Substances. – 2024. – Vol. 7, No. 1