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Journal articles on the topic 'Benzyl Benzoates'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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1

Yoh, Soo-dong, Duk-young Cheong, and Yuho Tsuno. "Alkaline hydrolysis of substituted benzyl substituted benzoates." Journal of Physical Organic Chemistry 6, no. 1 (1993): 23–28. http://dx.doi.org/10.1002/poc.610060105.

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2

E., M. ANAM, D. EKPA O., and V. GARIBOLDI P. "3-Isopropyl-9a-methyl-l ,2,4a,9a-tetrahydroxanthene, Benzyl Benzoates and Chamanen from Xylopia africana." Journal of Indian Chemical Society Vol. 71, April 1994 (1994): 179–81. https://doi.org/10.5281/zenodo.5894227.

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Chemistry Department, University of Calabar, P. M. B. 1115, Calabar, Cross River State, Nigeria Dipartimento di Science Chimiche, Universita di Camerino, 62032 Camerino (MC), Italy <em>Manuscript received 23 November 1992, revised 4 May 1993, accepted 3 June 1993</em> Dichloromethane extract of fresh roots of Xylopia africana (Annonaceae) gave four compounds, viz. 3-isopropyl-9\(\alpha\)-methyl-t,1,2,4a,9\(\alpha\)-tetrahydroxanthene (1), benzylbenzoate (2), <em>o</em>-methoxybenzylbenzoate (3) and chamanen (4). Compound J is reported for the first time from natural sources while compounds 2-4

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3

Song, Zhibin, Wei Huang, Yan Zhou, Zi-Qi Tian, Zhang-Min Li, and Duan-Jian Tao. "Thermally regulated molybdate-based ionic liquids toward molecular oxygen activation for one-pot oxidative cascade catalysis." Green Chemistry 22, no. 1 (2020): 103–9. http://dx.doi.org/10.1039/c9gc03646f.

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A family of thermally regulated molybdate-based ionic liquids has been developed for highly efficient synthesis of various flavones, imines, and benzyl benzoates through one-pot oxidative cascade catalysis.

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4

Zhu, Li, Xiyu Niu, and Xiaoquan Yao. "Selective oxidation of benzyl ethers to esters catalyzed by Cu₂O/C₃N₄ with TBHP & oxygen as co-oxidants." RSC Advances 15, no. 11 (2025): 8315–20. https://doi.org/10.1039/d4ra07724e.

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The Cu2O/C3N4 nanocomposite showed outstanding catalytic performance in the selective oxidation of benzyl ethers to benzoates, using TBHP and oxygen as co-oxidants, while significantly reducing the required amount of TBHP.

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5

Amiri-Attou, Ouassila, Thierry Terme, Maurice Médebielle, and Patrice Vanelle. "Original formation of benzyl benzoates by TDAE strategy." Tetrahedron Letters 49, no. 6 (2008): 1016–20. http://dx.doi.org/10.1016/j.tetlet.2007.12.011.

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6

Duanmu, Dandan, Pak-kin Leong, Qibai Jiang, and Hong Yan. "Pd(Ⅱ)-Catalyzed Synthesis of Benzyl Benzoates via Benzyl C(sp3)-H Activation." Chinese Journal of Organic Chemistry 37, no. 10 (2017): 2677. http://dx.doi.org/10.6023/cjoc201704040.

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7

Ma, Wen-Wen, Jon E. Anderson, and Jerry L. McLaughlin. "Bioactive Benzyl Benzoates from the Roots of Endlicheria Dysodantha." International Journal of Pharmacognosy 29, no. 3 (1991): 237–39. http://dx.doi.org/10.3109/13880209109082886.

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8

Kodpinid, M. "Benzyl benzoates and o-hydroxybenzyl flavanones from Uvaria ferruginea." Phytochemistry 23, no. 12 (1985): 3071–72. http://dx.doi.org/10.1016/s0031-9422(00)80643-3.

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9

Rivero-Cruz, Blanca, Isabel Rivero-Cruz, Rogelio Rodríguez-Sotres, and Rachel Mata. "Effect of natural and synthetic benzyl benzoates on calmodulin." Phytochemistry 68, no. 8 (2007): 1147–55. http://dx.doi.org/10.1016/j.phytochem.2007.02.026.

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10

Fang, Yuntai, Yaozong Chen, Guanfeng Feng, and Lin Ma. "Benzyl benzoates: New phlorizin analogs as mushroom tyrosinase inhibitors." Bioorganic & Medicinal Chemistry 19, no. 3 (2011): 1167–71. http://dx.doi.org/10.1016/j.bmc.2010.12.051.

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11

Kodpinid, Montree, Chachanat Thebtaranonth, and Yodhathai Thebtaranonth. "Benzyl benzoates and o-hydroxybenzyl flavanones from Uvaria ferruginea." Phytochemistry 24, no. 12 (1985): 3071–72. http://dx.doi.org/10.1016/0031-9422(85)80065-0.

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12

Lai, Ming, Xinxin Qi, and Xiao-Feng Wu. "Palladium-Catalyzed Carbonylative Synthesis of Benzyl Benzoates Employing Benzyl Formates as Both CO Surrogates and Benzyl Alcohol Sources." European Journal of Organic Chemistry 2019, no. 23 (2019): 3776–78. http://dx.doi.org/10.1002/ejoc.201900700.

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13

Bocharova, Oksana, Sentyabrina Reshta, and Vasiliy Eshtokin. "Toluene and Benzyl Alcohol Formation in Fruit Juices Containing Benzoates." Journal of Food Processing and Preservation 41, no. 4 (2016): e13054. http://dx.doi.org/10.1111/jfpp.13054.

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14

Huo, Yong-Wang, Le-Cheng Wang, Zhi-Peng Bao, A. Ru-Han, and Xiao-Feng Wu. "Nickel-catalyzed carbonylation of arylboronic acids and alkylarenes to benzyl benzoates." Journal of Catalysis 437 (September 2024): 115678. http://dx.doi.org/10.1016/j.jcat.2024.115678.

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15

Nkunya, M. H. H. "7-Methuljuglone, Diuvaretin, and Benzyl Benzoates from the Root Bark of Uvaria kirkii." Journal of Natural Products 48, no. 6 (1985): 999–1000. http://dx.doi.org/10.1021/np50042a028.

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16

Pfaff, Dominik, Gregor Nemecek, and Joachim Podlech. "A Lewis acid-promoted Pinner reaction." Beilstein Journal of Organic Chemistry 9 (August 2, 2013): 1572–77. http://dx.doi.org/10.3762/bjoc.9.179.

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Carbonitriles and alcohols react in a Lewis acid-promoted Pinner reaction to carboxylic esters. Best results are obtained with two equivalents of trimethylsilyl triflate as Lewis acid. Good yields are achieved with primary alcohols and aliphatic or benzylic carbonitriles, but the straightforward synthesis of acrylates and benzoates starting with acrylonitrile and benzonitrile, respectively, is similarly possible. Phenols are not acylated under these reaction conditions. The method has been used for the first total synthesis of the natural product monaspilosin. In the reaction of benzyl alcohol

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17

Saberi, Dariush, and Hajar Hashemi. "TBAI-catalyzed oxidative self-coupling of benzyl bromides under solvent-free conditions: A new pathway toward synthesis of benzyl benzoates." Catalysis Communications 106 (March 2018): 50–54. http://dx.doi.org/10.1016/j.catcom.2017.12.012.

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18

Kanjanapruk, Pitikarn, Therdsak Prammananan, Sathit Niratisai, and Kanawan Pochanakom. "Synthesis of Benzhydrol Derivatives as Antituberculosis Agents via Fries Rearrangement Method Investigated by DSC Analysis." Key Engineering Materials 914 (March 21, 2022): 141–46. http://dx.doi.org/10.4028/p-o6a9qa.

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Benzhydrol derivatives 2a-c were synthesized, and evaluated for antituberculosis activities. These compounds were prepared from corresponding phenyl benzoates through Fries rearrangement and reduction reaction. Fries rearrangement reaction was chosen to use due to its convenient non-solvent method for synthesis. In order to determine the effective temperature for Fries rearrangement reaction, the reaction mixtures of phenyl benzoates 4a-c and AlCl3 heated at constant rates were studied using DSC analysis. DSC curves of those mixtures showed that the reactions started at endothermic temperature

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19

Yoshida, Shuhei, Kenjiro Furuta, Kiyo Ashibe, et al. "Ethyl 4-[2-(Substituted Benzyl)hexyloxy]benzoates: Anti-Juvenile Hormone Agents with Juvenile Hormone Activity." Journal of the Faculty of Agriculture, Kyushu University 54, no. 1 (2009): 185–90. http://dx.doi.org/10.5109/14057.

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20

Patel, Brijesh H., and A. V. Doshi. "Mesomorphism and Molecular Structure: Novel Homologous Series 4-(4′-n-alkoxy cinnamoyloxy)-4′′-methoxy Benzyl Benzoates." Molecular Crystals and Liquid Crystals 607, no. 1 (2015): 78–86. http://dx.doi.org/10.1080/15421406.2014.930220.

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21

Patel, Brijesh H., and A. V. Doshi. "Synthesis and Liquid Crystal Properties of a Novel Homologous Series 4-(4′-n-Alkoxy benzoyloxy) Benzyl Benzoates." Molecular Crystals and Liquid Crystals 605, no. 1 (2014): 61–69. http://dx.doi.org/10.1080/15421406.2014.884399.

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22

Rivero-Cruz, Blanca, María Alejandra Rojas, Rogelio Rodríguez-Sotres, Carlos M. Cerda-García-Rojas, and Rachel Mata. "Smooth Muscle Relaxant Action of Benzyl Benzoates and Salicylic Acid Derivatives fromBrickellia veronicaefoliaon Isolated Guinea-Pig Ileum." Planta Medica 71, no. 4 (2005): 320–25. http://dx.doi.org/10.1055/s-2005-864097.

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23

Zhu, Hai-Tao, Xiao-Juan Tong, Ni-Ni Zhou, De-Suo Yang, and Ming-Jin Fan. "K2S2O8-promoted [2+2]-cycloaddition of benzyl-2-(3-hydroxypropynyl)-benzoates: A new route to polysubstituted cyclobutanes." Tetrahedron Letters 57, no. 49 (2016): 5497–500. http://dx.doi.org/10.1016/j.tetlet.2016.10.098.

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24

Satheesh, D., A. Rajendran, K. Chithra, and R. Saravanan. "Synthesis and antimicrobial evaluation of N1-benzyl/butyl-2-methyl-4-nitro-3-imidazolium 3΄-chloroperoxy benzoates." Chemical Data Collections 28 (August 2020): 100406. http://dx.doi.org/10.1016/j.cdc.2020.100406.

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25

Bocharova, Oksana. "Evaluation of the thermodynamic viability of the formation of benzyl alcohol and toluene from benzoates in milk and fruit yoghurts." International Journal of Dairy Technology 72, no. 4 (2019): 569–72. http://dx.doi.org/10.1111/1471-0307.12627.

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26

Mocerino, Mauro, and Robert V. Stick. "2-phenyl-1,3-benzodithiolylium trifluoromethanesulfonate: A reagent for the conversion of alcohols into benzyl ethers and benzoates under mild conditions." Tetrahedron Letters 31, no. 21 (1990): 3051–54. http://dx.doi.org/10.1016/s0040-4039(00)89023-1.

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27

Madahi, Meysam, Dadkhoda Ghazanfari, and Sayed Ali Ahmadi. "Theoretical Study of the Chemical Properties and the Reaction Pathway of Decarbonylative Alkylative Esterification of Styrenes with Aliphatic Aldehydes." Journal of Chemistry 2022 (February 18, 2022): 1–11. http://dx.doi.org/10.1155/2022/4842630.

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Using inexpensive and available aliphatic aldehydes as an alkyl source is a useful and cost-effective way to extend the chain of benzyl esters; this decarbonylative alkylative esterification of styrene derivatives has been used for organic synthesis and medical chemistry. A cocatalyzed decarbonylative alkylative esterification of styrene derivatives with aliphatic aldehydes and iodobenzenediacetate to provide chain elongated benzoates was investigated by the density functional theory, and quantum theory of atoms in molecules analysis has been used. The chemical properties and the reaction path

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28

MOCERINO, M., and R. V. STICK. "ChemInform Abstract: 2-Phenyl-1,3-benzodithiolylium Trifluoromethanesulfonate: A Reagent for the Conversion of Alcohols into Benzyl Ethers and Benzoates Under Mild Conditions." ChemInform 22, no. 23 (2010): no. http://dx.doi.org/10.1002/chin.199123246.

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29

Koval, A. S. "The choice of method of introduction of active substances into the basis of the cream for the treatment of acne and demodecosis." Farmatsevtychnyi zhurnal, no. 1 (February 17, 2021): 50–56. http://dx.doi.org/10.32352/0367-3057.1.21.06.

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Among dermatological diseases demodicosis and acne occupy a very important place. The incidence of demodicosis is more than 5% and ranks seventh in frequency among dermatological diseases. It is known that demodicosis can turn into acne. Treatment of demodicosis and acne does not lose its relevance. This medical problem can be solved through the development of the composition and technology of a soft drug of complex action with the content of active substances used to treat these diseases. Since in dermatology for external use the optimal soft medicines is a cream (taking into account th

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30

Desai, T., J. Gigg та R. Gigg. "The Allyl Group for Protection in Carbohydrate Chemistry. XXXI. Conversion of Allyl 2,6-Di-O-benzyl-α-D-galactopyranoside Into Allyl 2,6-Di-O-benzyl-α-D-glucopyranoside and 2,6-Di-O-benzyl-D-glucopyranose". Australian Journal of Chemistry 49, № 3 (1996): 305. http://dx.doi.org/10.1071/ch9960305.

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Allyl 2,6-di-O-benzyl-α-D-galactopyranoside was converted by tin-mediated alkylation into the 3-O-p-methoxybenzyl ether which gave the 4-O-mesyl derivative. Sodium benzoate in refluxing N,N-dimethylformamide converted the last compound into allyl 4-O-benzoyl-2,6-di-O-benzyl-3-O-p-methoxybenzyl-α-D-glucopyranoside in high yield. This was saponified and the product was treated with 2,3-dichloro-5,6-dicyano-1,4-benzoquinone to give the required allyl 2,6-di-O-benzyl-α-D-glucopyranoside whose structure was confirmed by conversion into the known 2,3,4,6-tetra-O-benzyl-D-glucopyranose. Removal of th

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31

&NA;. "Benzyl benzoate." Reactions Weekly &NA;, no. 305 (1990): 4. http://dx.doi.org/10.2165/00128415-199003050-00009.

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32

Gein, V. L., T. M. Zamaraeva, E. V. Gorgopina, and M. V. Dmitriev. "Biginelli reaction in the synthesis of ethyl 4-(6-aryl-5-benzoyl-4-hydroxy-2-thioxohexahydropyrimidine-4-carboxamido)benzoates." Журнал общей химии 93, no. 1 (2023): 43–49. http://dx.doi.org/10.31857/s0044460x23010055.

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Three-component Biginelli reaction of ethyl 4-(2,4-dioxo-4-phenylbutanamido)benzoate, aromatic aldehyde and thiourea in acetic acid in the presence of sodium acetate led to the formation of ethyl 4-(6-aryl-5-benzoyl4-hydroxy-2-thioxohexahydropyrimidine-4-carboxamido)benzoates. Structure of the obtained compounds was established by IR, 1H NMR, 13C spectroscopy methods.

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33

Doan, Chau Nguyen Minh, and Tin Thanh Nguyen. "STUDY OF THE CHEMICAL COMPOSITION IN LEAVES AND OIL OF Cananga odorata (Lam.) IN BEN TRE PROVINCE." Scientific Journal of Tra Vinh University 1, no. 40 (2020): 92–102. http://dx.doi.org/10.35382/18594816.1.40.2020.620.

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Investigation of the chemical composition of Cananga odorata(Lam.) leaves and essential oil in Ben Tre Province was conducted with steamenticing distillation method, extraction nhexane and Soxhlet with the solvents of nhexane, dietyl ether respectively. The results have determined the distillation conditions and the content of Cananga odorata (Lam.) essential oil by fresh weight and water volume is: 1: 3 (gram / ml)with distillation time: 3 to 4 hours. The content essential oil of Cananga odorata (Lam.) flower obtained in dry weight is 1.10% -1.26% and in fresh weight is 0.56% - 0.65%. The res

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34

Sriramavaratharajan, Venkatraman, and Ramar Murugan. "Chemical Profile of Leaf Essential Oil of Cinnamomum walaiwarense and Comparison of its Antioxidant and Hypoglycemic Activities with the Major Constituent Benzyl Benzoate." Natural Product Communications 13, no. 6 (2018): 1934578X1801300. http://dx.doi.org/10.1177/1934578x1801300633.

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Leaf essential oils of an unexplored wild cinnamon, Cinnamomum walaiwarense Kosterm. collected from seven different locations in the southern Western Ghats, India were characterized by GC-FID and GC-MS analyses. Benzyl benzoate was the principal constituent of the leaf essential oil present at a concentration from 65 to 89.8%. Another major constituent was phenylethyl benzoate. The results on antioxidant (ABTS and DPPH radical scavenging) and hypoglycemic (α-amylase and α-glucosidase inhibitory) activities show that the leaf essential oils exhibited better activities than benzyl benzoate. The

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35

Johnson, Wilbur, Wilma F. Bergfeld, Donald V. Belsito, et al. "Safety Assessment of Benzyl Alcohol, Benzoic Acid and its Salts, and Benzyl Benzoate." International Journal of Toxicology 36, no. 3_suppl (2017): 5S—30S. http://dx.doi.org/10.1177/1091581817728996.

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Benzyl alcohol, benzoic acid and its salts, and benzyl benzoate function mostly as fragrance ingredients/preservatives in cosmetic products. The Cosmetic Ingredient Review Expert Panel previously established concentration limits for benzyl alcohol, benzoic acid, and sodium benzoate in cosmetics and determined that the available data were insufficient to support the safety of these ingredients during inhalation exposure. After reviewing newly available data, it was concluded that benzyl alcohol, benzoic acid and its salts, and benzyl benzoate are safe in the present practices of use and concent

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36

Chitti Babu G, Kavita Dhar Bagati, Praveen Agarwal, and Jyostna Sharma. "A comparative study to assess the efficacy of permethrin (topical) and benzyl benzoate (topical) for the treatment of scabies patients." International Journal of Research in Pharmaceutical Sciences 10, no. 4 (2019): 3688–93. http://dx.doi.org/10.26452/ijrps.v10i4.1755.

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Several attempts have been made to come up with the anti-scabies drugs that are more efficient and safer. In India, scabies is more prevalent in overcrowded communities with low socioeconomic conditions, due to which the best efficient anti scabies drugs or treatment are unaffordable to them. To comparatively assess the efficacy of permethrin (topical) and benzyl benzoate (topical) in scabies patients. Study subjects with a confirmed diagnosis of scabies were included in this study. After enrolling 178 study subjects, they were equally distributed to two study groups (A & B) using a comput

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37

Poço, João Guilherme Rocha, Rodrigo Cella, and Silas Derenzo. "Improvements in the manufacture of benzoic acid obtained by catalytic oxidation of toluene." Journal of Engineering and Exact Sciences 10, no. 7 (2024): 20308. http://dx.doi.org/10.18540/jcecvl10iss7pp20308.

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This study investigates improvements in benzoic acid production through the catalytic oxidation of toluene with cobalt octoate. The oxidation process, which occurs under controlled conditions with temperatures ranging from 130 °C to 165 °C, typically results in a conversion rate of 50% toluene with a selectivity of 80% over benzoic acid. However, various by-products such as benzyl alcohol, benzaldehyde, and benzyl benzoate are also formed, which reduces the overall yield. The work identifies methods to minimize these byproducts, particularly benzyl benzoate, which forms in the distillation col

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38

Diastuti, Hartiwi, Mochammad Chasani, and Suwandri Suwandri. "Antibacterial Activity of Benzyl Benzoate and Crotepoxide from Kaempferia rotunda L. Rhizome." Indonesian Journal of Chemistry 20, no. 1 (2019): 9. http://dx.doi.org/10.22146/ijc.37526.

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Benzyl benzoate and crotepoxide are the major components of Kaempferia rotunda L. rhizome. However, the bioactivity study of benzyl benzoate and crotepoxide as the antibacterial activity were still limited. Therefore, the antibacterial activity of benzyl benzoate and crotepoxide against four pathogenic bacteria, i.e., Escherichia coli ATCC 25922, Enterococcus aerogenes ATCC 13048, Bacillus cereus ATCC 6538 and Staphylococcus aureus ATCC 11778 were investigated. The isolation steps were include the extraction by maceration with acetone, then the acetone extract was partitioned with n-hexane:met

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39

Hemmati Hassan Gavyar, Parvaneh, and Hamzeh Amiri. "CHEMICAL COMPOSITION OF ESSENTIAL OIL AND ANTIOXIDANT ACTIVITY OF Postia puberula, AN ENDEMIC SPECIES FROM IRAN." Acta Scientiarum Polonorum Hortorum Cultus 18, no. 1 (2019): 119–28. http://dx.doi.org/10.24326/asphc.2019.1.12.

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Essential oils from the leaves, stems and flowers of Postia puberula at the flowering stage were analyzed using GC and GC/MS. The results showed that leaves are abundant of cis-3-hexenyl benzoate (10.75%), benzyl benzoate (8.16%) and caryophyllene oxide (8.12%). The main compounds of stems were benzyl benzoate (21.92%), E-nuciferol (11.58%) and dibutyl phthalate (7.08%), while major components of flowers were benzyl benzoate (9.99%), caryophyllene oxide (8.14%) and E-nuciferol (8.13%). The antioxidant activities of methanol extract were evaluated by DPPH and β-carotene/linoleic acid assays. Th

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40

Mahdi, Omar, Hanaa Salih, and Abdullah Kshash. "Design, Synthesis of a Novel Banana-Shaped Compounds via Esterification." Diyala Journal For Pure Science 17, no. 4 (2021): 81–92. http://dx.doi.org/10.24237/djps.17.04.568c.

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Schiff's Bases were synthesized from the reaction of p-amino benzoic acid and alkoxybenzaldehyde in absolute ethanol and reacted with (E)-3-((4-hydroxybenzylidene) amino) phenol used DCC (N,N'-Dicyclocarbodiimide) and DAMP (4-(Dimethylamino) pyridine ) to 3-(((E)-4-((4-(((E)-4 alkoxy benzylidene) amino) benzoyl) oxy) benzylidene) amino) phenyl4- (E)- 4-alkoxy benzyli dene ) amino) benzoate. The structures of the products were confirmed by their melting points, FT-IR, 1HNMR spectra.

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41

Kutschy, Peter, Milan Dzurilla, Ladislav Kniežo, et al. "Reactions of 3-butine-2-methyl-2-ol with isothiocyanates." Collection of Czechoslovak Chemical Communications 51, no. 5 (1986): 1119–26. http://dx.doi.org/10.1135/cccc19861119.

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3-Butine-2-methyl-2-ol reacts with isothiocyanates in the presence of sodium hydride in dimethylformamide to give various products depending on structure of the isothiocyanate residue. Isothiocyanates with the NCS group bound to sp2 carbon atom (phenyl, 4-bromophenyl, and styryl isothiocyanates) give the respective 1,3-oxazolidine derivatives. If the NCS group is bound to an sp3-hybridized carbon atom (ethyl and benzyl isothiocyanates), derivatives of 1,3-oxathiolane are formed. Acyl isothiocyanates (benzoyl and 3-phenylpropenoyl isothiocyanates) give products of substitution of the NCS group,

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42

Hanna, Naeem B., Milena Masojídková, Pavel Fiedler, and Alois Pískala. "Synthesis of Some 6-Substituted 5-Azacytidines." Collection of Czechoslovak Chemical Communications 63, no. 2 (1998): 222–30. http://dx.doi.org/10.1135/cccc19980222.

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Protected 6-substituted benzyl, phenyl and chloromethyl derivatives of 5-azacytidine 8-10 have been prepared by addition of phenylacetyl- (2), benzoyl- (3) or (chloroacetyl)guanidine (4) to 2,3,5-tri-O-benzoyl-β-D-ribosyl isocyanate (1) and subsequent silylation-mediated cyclization of the obtained acyl(carbamoyl)guanidines 5-7. 4-Amino-6-phenyl-1,3,5-triazin-2(1H)-one (12) was obtained by condensation of carbamoylguanidine (13) with methyl benzoate in presence of methanolic sodium methoxide or by condensation of 13 with triethyl orthobenzoate in N,N-dimethylformamide. Stannic chloride catalyz

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43

Leka, Zorica, Sladjana B. Novaković, Goran A. Bogdanović, Gordana P. Radić, and Zoran R. Ratković. "Benzyl 2-(benzylsulfanyl)benzoate." Acta Crystallographica Section E Structure Reports Online 69, no. 2 (2013): o285—o286. http://dx.doi.org/10.1107/s1600536813001761.

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In the title compound, C21H18O2S, the central aromatic ring makes dihedral angles of 5.86 (12) and 72.02 (6)° with the rings of the terminalO-benzyl andS-benzyl groups, respectively. The dihedral angle between the peripheral phenyl rings is 66.16 (6)°. In the crystal, molecules are linked by pairs of C—H...O hydrogen bonds, forming inversion dimers. These dimers are linkedviaC—H...π interactions, forming a three-dimensional network.

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44

Ong, Gregory S. Y., Colin P. Somerville, Timothy W. Jones, and John P. Walsh. "Anaphylaxis Triggered by Benzyl Benzoate in a Preparation of Depot Testosterone Undecanoate." Case Reports in Medicine 2012 (2012): 1–3. http://dx.doi.org/10.1155/2012/384054.

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We report the first case of an anaphylactic reaction to Reandron 1000 (depot testosterone undecanoate with a castor oil and benzyl benzoate vehicle). While considered to have a favourable safety profile, serious complications such as oil embolism and anaphylaxis can occur. In our patient, skin testing identified benzyl benzoate to be the trigger, with no reaction to castor oil or testosterone undecanoate components. As benzyl benzoate exists in multiple pharmaceuticals, foods, and cosmetics, individual components of pharmaceuticals should be tested when investigating drug allergies. Doctors sh

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Xu, Xiao Feng, Qing Kang Zheng, and Jin Qu Zheng. "Effect of Carrier on the Structure and Performance of Polyphenylene Sulfide Fiber." Advanced Materials Research 554-556 (July 2012): 147–52. http://dx.doi.org/10.4028/www.scientific.net/amr.554-556.147.

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Polyphenylene sulfide (PPS) is considered as a high performance thermoplastic material and to be used in many areas, but the application of PPS used as protective clothing is limited because it is difficulties to be dyed and finished. In this work the effects of benzyl benzoate as a carrier on the structure and performance of PPS especially dyeability were evaluated. The glass transition temperature, crystalline structure and orientation degree of treated PPS fiber with benzyl benzoate were investigated by differential scanning calorimetry (DSC), X-ray diffraction analysis and velocity-oriente

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Taylor, George F., Maria K. Hristova-Kazmierski, F. Robert Ley, and John A. Kepler. "Synthesis of [benzyl-7-3H] and [benzoyl-7-14C] methyl 4-(2,5-dihydroxybenzylamino)benzoate." Journal of Labelled Compounds and Radiopharmaceuticals 38, no. 2 (1996): 187–92. http://dx.doi.org/10.1002/(sici)1099-1344(199602)38:2<187::aid-jlcr832>3.0.co;2-3.

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Emmanuel, Israel Edache, Samuel Hassan, Ishola Sulyman Yusuf, Arinze Okeh, and Ismaila Ayine Oba. "QSAR and Molecular Docking Analysis of Substituted Tetraketone and Benzyl-benzoate Analogs as Anti-tyrosine: A Novel Approach to anti-tyrosine kinase Drug Design and Discovery." Chemistry Research Journal 5, no. 6 (2020): 79–100. https://doi.org/10.5281/zenodo.13147551.

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<strong>Abstract </strong>In this paper, an attempt was made to develop a quantitative structure-activity relationship (QSAR) and molecular docking studies on a series of tetraketone and benzyl-benzoate Derivatives acting as protein tyrosine kinases (EGFR) inhibitors. QSAR was performed using the genetic algorithm-multiple linear regression (GA-MLR) method that comes out with a very promising result. According to Model-1 by GA-MLR anti-tyrosine activity of tetraketone and benzyl-benzoate derivatives were influenced by an individual (ATS0s, AATS6p, and VR1_Dze) and alignment independent descrip

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Jezdimirovic, Milanka, Nevenka Aleksic, and Biljana Radojicic. "Investigation of comparative efficacy of eugenol and benzyl benzoate in therapy of sheep mange." Veterinarski glasnik 64, no. 3-4 (2010): 177–85. http://dx.doi.org/10.2298/vetgl1004177j.

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The acaricide efficacy, tolerance and safety of eugenol (10 and 20 %) in the treatment of sarcoptic mange in sheep have been investigated. The results were compared with those corresponding for benzyl benzoate (25 %), which was applied to sheep in the same way. The treatment was applied on sheep three times in one-week intervals. Skin scrapings were sampled seven days after each treatment, as well as twenty-eight days following the third one. The changes on the skin were quantified and the mean recovery response (MRR) was calculated. The clinical efficacy was assessed according to the MRR and

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Atalay, Şehriman, and Ayşen Ağar. "Benzyl 2-(3,4-dicyanophenoxy)benzoate." Acta Crystallographica Section E Structure Reports Online 61, no. 6 (2005): o1815—o1817. http://dx.doi.org/10.1107/s1600536805014546.

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Chen, Ping-Shu, and Chin-Hsing Chou. "Pyrolytic Chemistry of Benzyl Benzoate." Journal of the Chinese Chemical Society 41, no. 5 (1994): 597–99. http://dx.doi.org/10.1002/jccs.199400080.

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