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Journal articles on the topic 'Phenol(methoxy-4)'

Author: Grafiati

Published: 4 June 2021

Last updated: 17 February 2022

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1

Lin, Zhi-Dong, Zhi-Dong Lin, Xing Li, and Ya-min Huang. "2-Methoxy-4-(phenyliminomethyl)phenol." Acta Crystallographica Section E Structure Reports Online 61, no. 9 (2005): o3032—o3033. http://dx.doi.org/10.1107/s1600536805026164.

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2

You, Xiu-Li, Yan Zhang, and De-Chun Zhang. "4-(2-Methoxy-4-nitrophenyldiazenyl)phenol monohydrate." Acta Crystallographica Section E Structure Reports Online 62, no. 2 (2006): o668—o670. http://dx.doi.org/10.1107/s1600536806001553.

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3

Li, Z. D., and G. Su. "2-Methoxy-5-(4-nitrostyryl)phenol." Acta Crystallographica Section C Crystal Structure Communications 51, no. 2 (1995): 311–13. http://dx.doi.org/10.1107/s0108270194008668.

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4

Ko˛sar, Bąsak, Çiğdem Albayrak, Mustafa Odabaşoğlu, and Orhan Büyükgüngör. "(E)-4-Methoxy-2-[(4-nitrophenyl)iminomethyl]phenol." Acta Crystallographica Section E Structure Reports Online 61, no. 7 (2005): o2106—o2108. http://dx.doi.org/10.1107/s1600536805018155.

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5

Perangin-angin, Sabarmin. "Synthesis Of 4-Alil-6- (Hydroxymethyl) -2-Methody Phenol Compounds from Eugenol Through Mannich Reaction Followed Methylation with Methyl Iodide and Subtitution Using NaOH." Journal of Chemical Natural Resources 1, no. 1 (2019): 75–85. http://dx.doi.org/10.32734/jcnar.v1i1.838.

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Eugenol derivative compound 4-allyl-6-hydroxymethyl-2-methoxy phenol was synthesized through Mannich reaction, methylation, dan nucleophilic substitution. Mannich reaction was carried out by reacting eugenol, formaldehyde 37%, and dimethylamine 40 % in reflux condition with n-heptane solvent at temperature 98o-100oC for 10 hours produced 4-allyl-6-(dimethylamino)methyl-2-methoxy phenol with yield of 83 %. The formation of dimethylaminomethyl group supported by C-N stretching vibration at 1246,16 cm-1 and ion molecule peak at 221 in GC-MS analysis. Methylation of 4-allyl-6-(dimethylamino)methyl

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6

Uçan, Selma, Aslı Öztürk, Nursabah Sarıkavaklı, and Tuncer Hökelek. "4-Methoxy-2-[(E)-(phenylimino)methyl]phenol." Acta Crystallographica Section E Structure Reports Online 64, no. 9 (2008): o1818—o1819. http://dx.doi.org/10.1107/s1600536808026883.

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7

Koşar, Başak, Arzu Özek, Çiğdem Albayrak, and Orhan Büyükgüngör. "(E)-4-Methoxy-2-(p-tolyliminomethyl)phenol." Acta Crystallographica Section E Structure Reports Online 66, no. 2 (2010): o469. http://dx.doi.org/10.1107/s1600536810003028.

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8

Özek, Arzu, Orhan Büyükgüngör, Çiğdem Albayrak, and Mustafa Odabaşoğlu. "(E)-4-Methoxy-2-(o-tolyliminomethyl)phenol." Acta Crystallographica Section E Structure Reports Online 65, no. 4 (2009): o791. http://dx.doi.org/10.1107/s1600536809009192.

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9

Khalaji, Aliakbar Dehno, Mahsa Nikookar, Karla Fejfarová, and Michal Dušek. "2-[(4-Methoxy-2-nitrophenyl)iminomethyl]phenol." Acta Crystallographica Section E Structure Reports Online 68, no. 8 (2012): o2445—o2446. http://dx.doi.org/10.1107/s1600536812031212.

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The crystal structure of the title compound, C14H12N2O4, contains four crystallographically independent molecules in the asymmetric unit. All the molecules have similar conformations; the dihedral angles between the aromatic rings are 33.1 (1), 33.76 (9), 31.41 (9) and 32.56 (10)°. Intramolecular O—H...N hydrogen bonds formS(6) ring motifs in each molecule. In the crystal, there are two pairs of pseudo-inversion-related molecules. Along thecaxis, molecules are stacked with π–π interactions between the 2-hydroxyphenyl and 4-methoxy-2-nitrophenyl rings [centroid–centroid distances = 3.5441 (12)–

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10

Zhou, Li-Na, Long Yan, Hui-Liang Zhou, Qing-Feng Yang, and Qi-Lin Hu. "2-Methoxy-4-[(4-methylpiperazin-1-yl)iminomethyl]phenol." Acta Crystallographica Section E Structure Reports Online 67, no. 1 (2010): o100. http://dx.doi.org/10.1107/s1600536810051135.

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11

Tahir, Muhammad, Siti Chuzaemi, Eko Widodo, and Hafsah Hafsah. "CHEMICAL COMPOUNDS AND ANTIOXIDANT CONTENTS OF CLOVES LEAVES ESSENTIAL OIL." AGROLAND The Agricultural Sciences Journal (e-Journal) 7, no. 1 (2020): 37–44. http://dx.doi.org/10.22487/agroland.v7i1.459.

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Essential oils from the distillation of clove leaves could act as anti-bacterial and anti-fungal agentsforeither food or feed. The purpose of this study was to identify chemical compounds and antioxidant content of clove leaves essential oils. The material used was clove leaves essential oil obtained by soxlet extraction. Clove leaves were taken from trees of over 10 years old in Palu, Central Sulawesi. Chemical compounds of the sample were analyzed by GC-MS method. Each peak that appeared on the chromatogram was identified by comparing to the standard. While the antioxidant analysis was carri

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12

Özdemir Tari, Gonca, Şamil Işık, Ramazan Özkan, and Ayşen Alaman Ağar. "3-Methoxy-2-[(E)-(4-methoxyphenyl)iminomethyl]phenol." Acta Crystallographica Section E Structure Reports Online 67, no. 2 (2011): o343—o344. http://dx.doi.org/10.1107/s1600536811000596.

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13

Keleşoğlu, Zeynep, Orhan Büyükgüngör, Çiğdem Albayrak, and Mustafa Odabaşoğlu. "(E)-4-Methoxy-2-[3-(trifluoromethyl)phenyliminomethyl]phenol." Acta Crystallographica Section E Structure Reports Online 65, no. 12 (2009): o3245—o3246. http://dx.doi.org/10.1107/s160053680905034x.

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14

Hashizume, Daisuke, Hiroyuki Koshino, In-Kyoung Lee, and Ick-Dong Yoo. "2,3,5-Trichloro-4-methoxy-6-[2,3,5-trichloro-4-methoxy-6-(2,3,5,6-tetrachloro-4-methoxyphenoxy)phenoxy]phenol." Acta Crystallographica Section E Structure Reports Online 61, no. 5 (2005): o1367—o1369. http://dx.doi.org/10.1107/s1600536805011220.

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15

Velázquez, Ana María, Luis Alberto Torres, Raúl González, et al. "Synthesis of 4-methoxy-2-thiomorpholin-4-ylmethyl-1-phenol." Molbank 2007, no. 3 (2007): M547. http://dx.doi.org/10.3390/m547.

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16

Dhahagani, K., K. Manvizhi, G. Chakkaravarthi, G. Anbalagan, and G. Rajagopal. "5-Methoxy-2-{[4-(morpholin-4-yl)phenyl]iminomethyl}phenol." Acta Crystallographica Section E Structure Reports Online 67, no. 9 (2011): o2501. http://dx.doi.org/10.1107/s1600536811034659.

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17

Purwono, Bambang, Chairil Anwar, and Ahmad Hanapi. "Syntheses of Azo-Imine Derivatives from Vanillin as an Acid Base Indicator." Indonesian Journal of Chemistry 13, no. 1 (2013): 1–6. http://dx.doi.org/10.22146/ijc.21318.

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Preparations of azo, imine and azo-imine derivatives from vanillin as an indicator of acid-base titration have been carried out. The azo derivative of 4-hydroxy-3-methoxy-5-(phenylazo)benzaldehyde 2 was produced by diazotitation reaction of vanillin in 37.04% yield. The azo product was then refluxed with aniline in ethanol to yield azo-imine derivatives, 2-methoxy-6-(phenylazo)-4-((phenylimino)methyl)phenol 1 in 82.21% yield. The imine derivative, 2-methoxy-4-((phenylimino)methyl)-phenol 3 was obtained by refluxing of vanillin and aniline mixture in ethanol solvent and produced 82.17% yield. T

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18

Sui, Xin Jin, and Shu Bin Wu. "Study on Mechanism of Action of Catalysts on Liquefaction of Bagasse Alkali Lignin." Advanced Materials Research 383-390 (November 2011): 6145–50. http://dx.doi.org/10.4028/www.scientific.net/amr.383-390.6145.

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Bagasse alkali lignin is the primary constituent of pulping black liquor. The phenolic products such as phenol, 2,6-dimethoxy-phenol and 2-methoxy-phenol were obtained by catalytic liquefaction from bagasse alkali lignin, with the aim of enhancing its use value. In the investigation, under optimal conditions, using SiO2-Al2O3 or FeS as catalyst, the phenols yield reached 54.10% and 55.18%, respectively. HPLC spectrum showed that the phenolic products of them were different. FT-IR and H-NMR spectrums showed that, using SiO2-Al2O3 as the catalyst, the α-O-4 and β-O-4 ether bonds and C-Cα bonds o

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19

Mao, Cheng-Gong, Shuang-Shuang Wang, Deng-Cheng Su, and Shao-Song Qian. "5-Bromo-2-methoxy-4-{[(4-methoxyphenyl)imino]methyl}phenol monohydrate." Acta Crystallographica Section E Structure Reports Online 68, no. 2 (2012): o249. http://dx.doi.org/10.1107/s1600536811054742.

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20

Li, He-Bing. "2-Methoxy-6-[(4-methylpyridin-2-yl)iminomethyl]phenol." Acta Crystallographica Section E Structure Reports Online 63, no. 11 (2007): o4246. http://dx.doi.org/10.1107/s1600536807048350.

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21

He, Gong Xiu, Dang Quan Zhang, Qi Mei Liu, and Kuan Peng. "450°C-Based Pyrolysis- GC/MS Analysis of Utilization of Benzene/Ethanol-Extracted Residue from Oil-Tea Cake." Key Engineering Materials 480-481 (June 2011): 472–77. http://dx.doi.org/10.4028/www.scientific.net/kem.480-481.472.

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The extractives of oil-tea cake are considered to have bioactive components, but the extracted residues of oil-tea cake are still not utilized. The analytical result by 450°C-based Pyrolysis-GC/MS showed that 42 peaks were obtained from the 450°C pyrolyzate of benzene/ethanol-extracted residues of oil-tea cake, and 41 compounds representing 97.53% of the total areas were identified. The analytical result revealed that the main components of benzene/ethanol-extracted residues of oil-tea cake by 450°C-based pyrolysis- GC/MS were as: Ethanone, 1-(2-Hydroxy-5-Methylphenyl)- (19.16%), Phenol, 2-Met

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22

Micheletti, Gabriele, Dario Telese, and Carla Boga. "3,5-Dimethoxy-2-[(4-methoxyphenyl)diazenyl]phenol." Molbank 2020, no. 3 (2020): M1152. http://dx.doi.org/10.3390/m1152.

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3,5-Dimethoxy-2-[(4-methoxyphenyl)diazenyl]phenol was synthesized by an azo-coupling reaction between 3,5-dimethoxyphenol and 4-methoxy benzenediazonium tetrafluoroborate. The structure of newly synthesized compound was elucidated based on 1H NMR, 13C NMR, ESI-MS, UV-Vis and FT-IR.

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23

Sukria, L., E. K. Hayati, A. Hanapi, R. Adawiyah, and R. Ningsih. "Anticancer activity in 2-methoxy-4-((4-methoxy-phenilimino)-methyl)-phenol compound on T47D breast cancer cells." IOP Conference Series: Earth and Environmental Science 456 (April 8, 2020): 012014. http://dx.doi.org/10.1088/1755-1315/456/1/012014.

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24

Kantar, Esen Nur, Yavuz Köysal, Mustafa Macit, Ebru Er, and Mustafa Serkan Soylu. "4-Methoxy-2-{(E)-[(thiophen-2-yl)methylimino]methyl}phenol." Acta Crystallographica Section E Structure Reports Online 68, no. 9 (2012): o2801. http://dx.doi.org/10.1107/s1600536812036586.

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25

IYER, M. R., S. BASKARAN, and G. K. TRIVEDI. "ChemInform Abstract: Oxidative Studies on trans-(3-Phenyl-2-propenyl)phenols and 2-Methoxy- 4-(2-propenyl)phenol and 2-Methoxy-4-(1-propenyl)phenol." ChemInform 26, no. 40 (2010): no. http://dx.doi.org/10.1002/chin.199540270.

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26

Suryanto, Edi, Mercy R. I. Taroreh, and Lydia Irma Momuat. "Purification and Characterization of Phenolic Antioxidant from Corncob Liquid Smoke." Asian Journal of Chemistry 32, no. 12 (2020): 2985–90. http://dx.doi.org/10.14233/ajchem.2020.22486.

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This study aimed to purify and characterize the antioxidant activity of liquid smoke acquired from corncobs. The smoke of crude liquids was generated through pyrolysis and was purified through fractional and simple distillation. The liquid smoke was analyzed using crude fibres, cellulose, hemicellulose, lignin, antioxidant activity and total phenolic compounds. Gas chromatography-mass spectrometry (GC-MS) was employed to analyze the volatile compounds of liquid smoke. Fractional distillation exhibited the higher carbonyl and phenol content than simple distillation, and the overall acid content

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27

Şahin, Onur, Orhan Büyükgüngör, Mustafa Odabaşoğlu, and Çiğdem Albayrak. "Crystallographic and conformational analyses of (E)-4-methoxy-2-((4-methoxyphenylimino)methyl)phenol." Acta Crystallographica Section A Foundations of Crystallography 65, a1 (2009): s262—s263. http://dx.doi.org/10.1107/s0108767309094501.

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28

Zhang, Dang Quan, Huai Yun Zhang, Lin Lin Guo, and Kuan Peng. "Determination of Bioactive Components of Acetone Extractives of Cinnamomum camphora Root Wood by Py-GC/MS under 350°C." Advanced Materials Research 230-232 (May 2011): 837–41. http://dx.doi.org/10.4028/www.scientific.net/amr.230-232.837.

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Py-GC/MS technology was used to analyze the high-grade resource recovering approaches of C. camphora root wood at 350°C. The result showed that the chemical components of acetone extractives from C. camphora root wood are as: Benzene, 1,2-dimethoxy-4-(2-propenyl)- (10.255%), Bicyclo[2.2.1]heptan-2-one, 1,7,7-trimethyl-, (1R)- (7.751%), p-menth-1-en-8-ol (5.765%), Phenol, 2,6-dimethoxy-4-(2-propenyl)- (3.833%), 1,6-Cyclodecadiene, 1-methyl-5-methylene-8- (1-methylethyl)-, [s-(E,E)]- (3.669%), D-Allose (3.265%), Acetic acid (2.784%), 1(2H)-Naphthalenone, octahydro-8a-hydroxy- (2.719%), 1,3-Benzo

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29

DJIELE, Patrice, Bernhard WALFORT, and Heinrich LANG. "Solid-State Structure of 2-[1-4(Methoxy-phenylimino)ethyl]phenol." Analytical Sciences: X-ray Structure Analysis Online 21 (2005): x37—x38. http://dx.doi.org/10.2116/analscix.21.x37.

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30

Mills-Robles, Heather A., Vasumathi Desikan, James A. Golen, and David R. Manke. "Crystal structure of 3,4-dimethoxyphenol." Acta Crystallographica Section E Crystallographic Communications 71, no. 12 (2015): o1019. http://dx.doi.org/10.1107/s2056989015022860.

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The title compound, C8H10O3, has two planar molecules in the asymmetric unit possessing mean deviations from planarity of 0.051 and 0.071 Å. In the crystal, there are two distinct infinite chains, both along [010]. The chains are formed by O—H...O interactions between the phenol and both the 3-methoxy and the 4-methoxy groups.

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31

Oramahi, Hasan Ashari, Tsuyoshi Yoshimura, Elvi Rusmiyanto, and Kustiati Kustiati. "Optimization and Characterization of Wood Vinegar Produced by Shorea laevis Ridl Wood Pyrolysis." Indonesian Journal of Chemistry 20, no. 4 (2020): 825. http://dx.doi.org/10.22146/ijc.45783.

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In this study, the Box-Behnken Design (BBD) was employed to investigate the effects of wood particle size, pyrolysis temperature, and pyrolysis time on the production of wood vinegar from Indonesia “bengkirai” wood (Shorea laevis Ridl). Characterization of wood vinegar was conducted by gas chromatography-mass spectrometry (GC-MS). Three variable designs consisting of wood particle size (2.00, 2.38, and 3.36 mm), pyrolysis temperature (350, 400, and 450 °C), and pyrolysis time (105, 120, and 135 min) were employed in a BBD response surface methodology (RSM-BBD). RSM-BBD results suggested that m

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32

Li, Qing, Kuan Peng, and Dang Quan Zhang. "Determination of Bioactive Components of 600 °C Pyrolyzate from Acetone/Ethanol Extractives of Moso Bamboo Root by Pyrolysis-GC/MS." Key Engineering Materials 480-481 (June 2011): 484–89. http://dx.doi.org/10.4028/www.scientific.net/kem.480-481.484.

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The bioactive components of acetone/ethanol extractives of Moso bamboo root was identified by 600°C-based Pyrolysis-GC/MS. 45 compounds representing 96.31 % of the total areas were identified from these 47 peaks. The main components in the 600°C pyrolyzate of benzene/methanol extractives of Moso bamboo root by Pyrolysis- GC/MS analysis are as: Phenol, 2,6-Dimethoxy- (12.58%), 4-Hydroxy-2-Methylacetophenone (9.53%), 3',5'-Dimethoxy- acetophenone (8.15%), Mequinol (7.84%), 2-Propenoic Acid, 3-(2-Hydroxyphenyl)-,(E)- (7.49%), .Gamma.-Sitosterol (3.62%), 1,3-Benzodioxole, 5-(1-Propenyl)- (3.61%),

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33

Jumina, Jumina, Evi Triwulandari, and Chairil Anwar. "SYNTHESIS OF C-METHYL-4,10,16,22-TETRAMETHOXYCALIX[4]ARENE FROM PHENOL USING BF3-METHANOL AS THE CATALYST." Indonesian Journal of Chemistry 5, no. 1 (2010): 58–65. http://dx.doi.org/10.22146/ijc.21840.

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C-Methyl 4,10,16,22-tetramethoxycalix[4]arene has been synthesized from phenol. The reaction performed consisted of methylation of phenol, acetylation of methyl phenyl ether, reduction of p-methoxyacetophenone, and cyclization of p-methoxy-(1-hydroxyethyl)benzene to form C-methyl-4,10,16,22-tetramethoxycalix[4]-arene using BF3-methanol as the acid catalyst. Methylation of phenol was done by reacting phenol with solution of NaOH to generate sodium phenoxide salt. This mixture was strirred at reflux for 0.5 hours. Dimethyl sulphate was added and the reflux was continued for 2,5 hours. The produc

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34

Khanra, Somnath, Sabyasachi Ta, Milan Ghosh, Sudeshna Chatterjee, Pallabi Mukherjee, and Debasis Das. "Al3+ triggered aggregation induced emission of an anthracence based azine derivative in SDS medium." New Journal of Chemistry 44, no. 20 (2020): 8477–85. http://dx.doi.org/10.1039/d0nj00968g.

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Single crystal X-ray structurally characterized anthracene appended unsymmetrical azine derivative, viz. 4-(anthracen-9-ylmethylene-hydrazonomethyl)-2-methoxy-phenol (L5) shows Al<sup>3+</sup> assisted aggregation induced emission in SDS medium.

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35

Deacon, GB, MJ Oconnor, and GN Stretton. "Organomercury Compounds .XXVIII. The Synthesis and 199Hg N.M.R-Spectra of Some Unsymmetrically Dimercurated Arenes." Australian Journal of Chemistry 39, no. 7 (1986): 953. http://dx.doi.org/10.1071/ch9860953.

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Mercuration of 1-methoxy-2-nitrobenzene (1) with mercuric trifluoroacetate (mole ratio 1 : 1) in trifluoroacetic acid yields 1- methoxy-2-nitro-4-(trifluoroacetatomercurio)benzene (2). With a 1 : 2 mole ratio, (2) and 1-methoxy-2-nitro-4,6- bis(trifluoroacetatomercurio)benzene (3) are obtained, and, with a 1:4 ratio, (3) and a little 1-methoxy-2-nitro-3,4- bis(trifluoroacetatomercurio)benzene (4). are obtained. 2-Nitrophenol (5) with mercuric trifluoroacetate (mole ratio 1 : 2) gives 2-nitro- 4,6-bis(trifluoroacetatomercurio)phenol (6), and vanillin (7) yields 5,6-bis(trifluoroacetatomercurio)

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36

Zhang, Jin, Ying Tang, Jia-Qing Xie, Jian-Zhang Li, Wei Zeng, and Chang-Wei Hu. "Study on phenol oxidation with H2O2." Journal of the Serbian Chemical Society 70, no. 10 (2005): 1137–46. http://dx.doi.org/10.2298/jsc0510137z.

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Two new ligands, 1-hydroxy-5- 4-(2-hydroxybenzylideneamino)pheno - xy -3-oxapentane (HL1) and 1-methoxy-5- 4-(2-hydroxybenzylideneamino)pheno - xy -3-oxapentane (HL2), and their Mn(III) complexes were synthesized and characterized. The two new Schiff base Mn(III) complexes were used to mimic peroxidase in the oxidation of phenol by hydrogen peroxide. The effect of the mole ratio of H2O2 to the complex, pH and temperature on the reaction rate was investigated. The mechanism of the catalytic oxidation is discussed. A kinetic mathematic model for the oxidation of phenol catalyzed by Schiff base M

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37

Zhao, Shunsheng, Xiangrong Liu, Xingqiang Lü, and Weixu Feng. "4-Bromo-2-methoxy-6-(1-phenyl-1H-benzimidazol-2-yl)phenol." Acta Crystallographica Section E Structure Reports Online 68, no. 3 (2012): o852. http://dx.doi.org/10.1107/s1600536812007313.

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38

Hong, Yong. "Crystal structure of (E)-2-bromo-4-chloro-6-(4-methoxy-2-nitrostyryl)phenol, C14H10BrClN2O4." Zeitschrift für Kristallographie - New Crystal Structures 233, no. 4 (2018): 663–64. http://dx.doi.org/10.1515/ncrs-2017-0426.

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39

Ajibade, Peter A., and Fartisincha P. Andrew. "4-(((4-Methoxyphenyl)amino)methyl)-N,N-dimethylaniline and 2-Methoxy-5-((phenylamino)methyl)phenol." Molbank 2021, no. 3 (2021): M1274. http://dx.doi.org/10.3390/m1274.

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Molecular structures of 4-(((4-methoxyphenyl)amino)methyl)-N,N-dimethylaniline and 2-methoxy-5-((phenylamino)methyl)phenol synthesized via Schiff bases reduction route are reported. The compounds consist of asymmetric units of C16H20N2O (1) and C14H15NO2 (2) in orthorhombic and monoclinic crystal systems, respectively. Compound 1 consist of intermolecular C11—H11···N2 hydrogen bonding with C11···N21 = 3.463(4) Å. The hydroxyl group in 2 is also involved in intermolecular O2—H2···O2 and O2—H2···O21 hydrogen bonding with O2···O11 = 2.8885(15) Å and O1···O21 = 2.9277(5) Å. The molecular structure

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40

Hernawan, Hernawan, Bambang Purwono, and Tutik Dwi Wahyuningsih. "SYNTHESIS OF 2-METHOXY-4,6-DI(PROP-1-ENYL)PHENOL FROM EUGENOL AND ITS ACTIVITY AS AN ANTIOXIDANT." Indonesian Journal of Chemistry 12, no. 2 (2012): 178–83. http://dx.doi.org/10.22146/ijc.21360.

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Synthesis and antioxidant activity of 2-methoxy-4,6-di(prop-1-enyl) phenol from eugenol have been investigated. Synthesis was conducted through three stages of reaction. The first step was CTAB micellar catalytic O-allylation reaction at room temperature, to give 4-allyl-1-(allyloxy)-2-methoxybenzene (2). Compound (2) was subsequently heated for Claisen rearrangement and produced 2,4-diallyl-6- methoxyphenol (3). The final steps was isomerization of compound (3) in alkaline conditions in ethylene glycol, to yield 2-methoxy-4,6-di(prop-1-enyl) phenol (4). Antioxidant activity test was conducted

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41

Panda, Gautam, Jitendra Kumar Mishra, Sudhir Sinha, et al. "4-[10-(Methoxy-benzyl)-anthracen-9-yl]-phenol derivatives as new antitubercular agents." Arkivoc 2005, no. 2 (2005): 29–45. http://dx.doi.org/10.3998/ark.5550190.0006.204.

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42

Miura, Yukie, Yoshikazu Aritake, and Takashiro Akitsu. "A chiral photochromic Schiff base: (R)-4-methoxy-2-[(1-phenylethyl)iminomethyl]phenol." Acta Crystallographica Section E Structure Reports Online 65, no. 10 (2009): o2381. http://dx.doi.org/10.1107/s1600536809035557.

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43

Vaghasiya, Yogesh, Rathish Nair, Mayur Soni, Shipra Baluja, and Sumitra Shanda. "Synthesis, structural determination and antibacterial activity of compounds derived from vanillin and 4-aminoantipyrine." Journal of the Serbian Chemical Society 69, no. 12 (2004): 991–98. http://dx.doi.org/10.2298/jsc0412991v.

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Schiff bases derived from 4-aminoantipyrine and vanillin were evaluated for their potential as antibacterial agents against some Gram positive and Gram negative bacterial strains. The antibacterial activity was studied against P. pseudoalcaligenes ATCC 17440, P. vulgaris NCTC 8313, C. freundii ATCC 10787 E. aerogenes ATCC 13048, S. subfava NCIM 2178 and B. megaterium ATCC 9885. The determination of the antibacterial activity was done using the Agar Ditsh method. The Schiff bases produced were: (1) 4-(4-hydroxy 3-methoxybenzylideneamino) -1,5-dimethyl-2-phenyl-1,2-dihydro-pyrazol-3-one [VV1]; (

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44

Eseyin, Anthonia E., El Barbary Hassan, and Emad, M. El-Giar. "Comparative analyses of Nigerian and US corn Stalks, using PY-GC/MS." International Journal of Advanced Chemistry 3, no. 1 (2015): 18. http://dx.doi.org/10.14419/ijac.v3i1.4328.

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<p>Pyrolysis gas chromatography mass spectrometry (Py-GC/MS) studies were carried out on the Nigerian and US corn stalks at 500 °C. Analyses of the fast pyrolysis products showed that the Nigerian corn stalks produced more diverse compounds like: acetaldehyde, acetic acid methyl ester, 2,3-pentanedione, 1-hydroxy-2-butanone, butanedial, phenol and vanillin. On the other hand, the pyrolyzed US corn stalks produced compounds like: furfural, phenol, 2-methoxy, 2-methylbenzaldehyde, and 2-methoxy-4-vinylphenol which had significantly high peak area percentages. Few anhydrous sugars were dete

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45

Liu, Jian-Feng, Hui-Duo Xian та Guo-Liang Zhao. "Tris{2-methoxy-6-[(4-methylphenyl)iminiomethyl]phenolato-κ2O,O′}tris(thiocyanato-κN)cerium(III)". Acta Crystallographica Section E Structure Reports Online 65, № 6 (2009): m650. http://dx.doi.org/10.1107/s1600536809016808.

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The asymmetric unit of the title compound, [Ce(NCS)3(C15H15NO2)3], contains three Schiff base 2-methoxy-6-[(4-methylphenyl)iminomethyl]phenol (HL) ligands and three independent thiocyanate ions that coordinate the cerium ionviatheir N atoms. The protonated imine N atoms are involved in an intramolecular hydrogen bond with the respective phenoxide group. The Ce(III) ion exhibits a coordination number of nine.

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46

Huang, Yuan, Yaru Qin, Yu Ge, et al. "Rationally assembled nonanuclear lanthanide clusters: Dy9 displays slow relaxation of magnetization and Tb9 serves as luminescent sensor for Fe3+, CrO42− and Cr2O72−." New Journal of Chemistry 43, no. 48 (2019): 19344–54. http://dx.doi.org/10.1039/c9nj04893f.

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The utilization of a Schiff base ligand 2-((2-hydroxy-4-methoxy-benzylideneamino)methyl)phenol (H<sub>2</sub>L) afforded five nonanuclear lanthanide(iii) clusters. Dy<sub>9</sub> displays slow relaxation of magnetization and Tb<sub>9</sub> serves as luminescent sensor for Fe<sup>3+</sup>, CrO<sub>4</sub><sup>2−</sup> and Cr<sub>2</sub>O<sub>7</sub><sup>2−</sup>.

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47

Han, J. K., J. Miltz, B. R. Harte, J. R. Giacin, and J. I. Gray. "Loss of 2-tertiary-butyl-4-methoxy phenol (BHA) from high-density polyethylene film." Polymer Engineering and Science 27, no. 13 (1987): 934–38. http://dx.doi.org/10.1002/pen.760271303.

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48

Adam, Farook, Md Azharul Arafath, Rosenani Anwaeul Haque, and Mohd Rizal Razali. "Crystal structure of (E)-4-methoxy-2-{[(5-methylpyridin-2-yl)imino]methyl}phenol." Acta Crystallographica Section E Crystallographic Communications 71, no. 11 (2015): o819. http://dx.doi.org/10.1107/s2056989015018113.

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The molecule of the title Schiff base compound, C14H14N2O2, displays anEconformation with respect the imine C=N double bond. The molecule is approximately planar, with the dihedral angle formed by the planes of the pyridine and benzene rings being 5.72 (6)°. There is an intramolecular hydrogen bond involving the phenolic H and imine N atoms.

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49

Upadhyay, Apoorva, Chinmoy Das, Stuart K. Langley, Keith S. Murray, Anant K. Srivastava, and Maheswaran Shanmugam. "Heteronuclear Ni(ii)–Ln(iii) (Ln = La, Pr, Tb, Dy) complexes: synthesis and single-molecule magnet behaviour." Dalton Transactions 45, no. 8 (2016): 3616–26. http://dx.doi.org/10.1039/c5dt04102c.

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The crystal structures are reported for three heterometallic Ni<sub>2</sub>Ln and a Ni<sub>2</sub>Dy<sub>2</sub> complex, using the Schiff base ligand 2-methoxy-6-[(E)-phenyliminomethyl] phenol. Detailed dc and ac magnetic susceptibility studies were reported for all the complexes. The complexes 3 and 4 shows frequency dependent out-of-phase susceptibility signals.

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50

Collins, DJ, and HA Jacobs. "Synthesis of 3-(4′-Methoxyphenyl)-2,2,4,4-Tetramethylpentane and Some Cyclic Analogs." Australian Journal of Chemistry 39, no. 12 (1986): 2095. http://dx.doi.org/10.1071/ch9862095.

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Reaction of 1-methoxy-2-methyl-1-trimethylsilyloxyprop-1-ene (8) with 1-acetoxy-1-(4′-methoxyphenyl)-2,2-dimethylpropane (7b) in the presence of zinc iodide gave 84% of methyl 3-(4′methoxyphenyl)-2,2,4,4- tetramethylpentanoate (9a), which was reduced with lithium aluminium hydride to 3-(4′-methoxyphenyl)-2,2,4,4-tetramethylpentan-1-ol(12a). Hydride reduction of the derived tosylate (12b) afforded 3-(4′-methoxyphenyl )-2,2,4,4-tetramethylpentane (5b) which upon demethylation yielded the corresponding phenol (10a). In an analogous manner, 1-acetoxy-1-(4′-methoxyphenyl)-2-methylpropane (7d) was c

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