Relevant bibliographies by topics / Ethoxybenzoic Acid

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  1. Journal articles

Academic literature on the topic 'Ethoxybenzoic Acid'

Author: Grafiati
Published: 3 June 2025
Last updated: 31 July 2025

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Journal articles on the topic "Ethoxybenzoic Acid"

1

Fujisawa, S., T. Atsumi, K. Satoh, and H. Sakagami. "Interaction between 2-Ethoxybenzoic Acid (EBA) and Eugenol, and Related Changes in Cytotoxicity." Journal of Dental Research 82, no. 1 (2003): 43–47. http://dx.doi.org/10.1177/154405910308200110.

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The liquid of 2-ethoxybenzoic acid cements is composed of 2-ethoxybenzoic acid and eugenol (4-allyl-2-methoxyphenol). Recently, eugenol was reported to produce radicals at a higher pH, which consequently directly damages cells. We examined here whether eugenol radicals are generated from the mixture of eugenol/calcium hydroxide, and also whether 2-ethoxybenzoic acid or acetylsalicylic acid scavenges radicals, using electron spin resonance spectroscopy. Radicals were generated from the mixture of eugenol/calcium hydroxide in 50% dimethylsulfoxide solution. The radical intensity of eugenol in 50
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2

Waisser, Karel, Jiří Kuneš, Jiří Klimeš, Miroslav Polášek, and Želmíra Odlerová. "Relations between Structure and Antituberculotic Activity of 4-Alkoxybenzoic Acids." Collection of Czechoslovak Chemical Communications 58, no. 1 (1993): 191–96. http://dx.doi.org/10.1135/cccc19930191.

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Antimycobacterial activity of a series of alkoxybenzoic acids including 4-methoxybenzoic acid (II), 4-ethoxybenzoic acid (III), 4-propoxybenzoic acid (IV), 4-butoxybenzoic acid (V), 4-pentoxybenzoic acid (VI), 4-allyloxybenzoic acid (IX), 4-isopropoxybenzoic acid (VII), 4-isobutoxybenzoic acid (VIII) and 4-benzyloxybenzoic acid (X) has been determined and found to increase with the lipophilicity of the compounds expressed by the corresponding HPLC capacity factors. Also determined were the pKa values of the compounds mentioned. The most active compound, 4-pentoxybenzoic acid (VI), is comparabl
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3

Tabuchi, Yohei, Kazuma Gotoh, and Hiroyuki Ishida. "Crystal structures of three co-crystals of 1,2-bis(pyridin-4-yl)ethane with 4-alkoxybenzoic acids: 4-ethoxybenzoic acid–1,2-bis(pyridin-4-yl)ethane (2/1), 4-n-propoxybenzoic acid–1,2-bis(pyridin-4-yl)ethane (2/1) and 4-n-butoxybenzoic acid–1,2-bis(pyridin-4-yl)ethane (2/1)." Acta Crystallographica Section E Crystallographic Communications 71, no. 11 (2015): 1340–44. http://dx.doi.org/10.1107/s2056989015019349.

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The crystal structures of three hydrogen-bonded co-crystals of 4-alkoxybenzoic acid–1,2-bis(pyridin-4-yl)ethane (2/1), namely, 2C9H10O3·C12H12N2, (I), 2C10H12O3·C12H12N2, (II), and 2C11H14O3·C12H12N2, (III), have been determined at 93, 290 and 93 K, respectively. In (I), the asymmetric unit consists of one 4-ethoxybenzoic acid molecule and one half-molecule of 1,2-bis(pyridin-4-yl)ethane, which lies on an inversion centre. In (II) and (III), the asymmetric units each comprise two crystallographically independent 4-alkoxybenzoic acid molecules and one 1,2-bis(pyridin-4-yl)ethane molecule. In ea
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4

Wei, Tai-Bao, You-Ming Zhang, Hai Wang, and Li-Ming Gao. "PHASE TRANSFER CATALYZED SYNTHESIS OF THIOSEMICARBAZIDE AND bis-THIOSEMICARBAZIDE DERIVATIVES OF 2-ETHOXYBENZOIC ACID." Phosphorus, Sulfur, and Silicon and the Related Elements 179, no. 8 (2004): 1539–44. http://dx.doi.org/10.1080/10426500490464078.

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5

Campbell, Mariya, Chih-Yun Cho, Andrew Ho, Jye-Yu Huang, Brooke Martin, and Eric S. Gilbert. "4-Ethoxybenzoic acid inhibits Staphylococcus aureus biofilm formation and potentiates biofilm sensitivity to vancomycin." International Journal of Antimicrobial Agents 56, no. 3 (2020): 106086. http://dx.doi.org/10.1016/j.ijantimicag.2020.106086.

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6

Lai, L. L., L. J. Lee, D. W. Luo, Y. H. Liu, and Y. Wang. "Single crystal XRD study of 4,4′-dipyridyl — p-ethoxybenzoic acid and N,N′-dipyridylpiperazine — p-ethoxybenzoic acid co-crystals: Direct evidence of H-bond interaction in the corresponding liquid-crystalline mesogenic phases." Journal of Structural Chemistry 49, no. 6 (2008): 1137–40. http://dx.doi.org/10.1007/s10947-008-0193-2.

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7

Moretton, Tod R., Cecil E. Brown, Joseph J. Legan, and A. H. Kafrawy. "Tissue reactions after subcutaneous and intraosseous implantation of mineral trioxide aggregate and ethoxybenzoic acid cement." Journal of Biomedical Materials Research 52, no. 3 (2000): 528–33. http://dx.doi.org/10.1002/1097-4636(20001205)52:3<528::aid-jbm11>3.0.co;2-9.

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8

James, Bruce D., Loretta M. Kivlighon, Brian W. Skelton, and Allan H. White. "Triphenyltin(IV) compounds with biologically active anionic groups: Crystal and molecular structures of thep-ethoxybenzoic acid, acetylsalicylic acid, phthalic acid and salicylaldehyde derivatives." Applied Organometallic Chemistry 12, no. 1 (1998): 13–23. http://dx.doi.org/10.1002/(sici)1099-0739(199801)12:1<13::aid-aoc648>3.0.co;2-4.

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9

Iliescu, Alexandru Andrei, Cristian Marian Petcu, Ileana Cristiana Petcu, et al. "Tissue Reaction to Subcutaneous Implantation of SuperEBA (Reinforced Zinc Oxide Cement) Used as Root-End Filling Material: A Histological Study in Rats." Key Engineering Materials 695 (May 2016): 247–51. http://dx.doi.org/10.4028/www.scientific.net/kem.695.247.

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The retrograde filling is a critical step to a successful outcome of the endodontic surgery. Despite the progress in the technology of novel root-end filling materials, zinc oxide-eugenol cement superEBA is still preserving its clinical value on long-term basis. The study aimed to reconsider the tissue response to the initial irritating effect of this material. Silicon tubes filled with superEBA were subcutaneously implanted for 120 days in white Wistar rats which were afterwards sacrificed. The connective tissue surrounding the superEBA implants revealed fibroblast proliferation and a definit
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10

Tabuchi, Yohei, Kazuma Gotoh, and Hiroyuki Ishida. "Crystal structures of four co-crystals of (E)-1,2-di(pyridin-4-yl)ethene with 4-alkoxybenzoic acids: 4-methoxybenzoic acid–(E)-1,2-di(pyridin-4-yl)ethene (2/1), 4-ethoxybenzoic acid–(E)-1,2-di(pyridin-4-yl)ethene (2/1), 4-n-propoxybenzoic acid–(E)-1,2-di(pyridin-4-yl)ethene (2/1) and 4-n-butoxybenzoic acid–(E)-1,2-di(pyridin-4-yl)ethene (2/1)." Acta Crystallographica Section E Crystallographic Communications 72, no. 11 (2016): 1666–71. http://dx.doi.org/10.1107/s2056989016017138.

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The crystal structures of four hydrogen-bonded co-crystals of 4-alkoxybenzoic acid–(E)-1,2-di(pyridin-4-yl)ethene (2/1), namely, 2C8H8O3·C12H10N2, (I), 2C9H10O3·C12H10N2, (II), 2C10H12O3·C12H10N2, (III) and 2C11H14O3·C12H10N2, (IV), have been determined at 93 K. In compounds (I) and (IV), the asymmetric units are each composed of one 4-alkoxybenzoic acid molecule and one half-molecule of (E)-1,2-di(pyridin-4-yl)ethene, which lies on an inversion centre. The asymmetric unit of (II) consists of two crystallographically independent 4-ethoxybenzoic acid molecules and one 1,2-di(pyridin-4-yl)ethene
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