Academic literature on the topic 'Phenol(methoxy-4)'

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

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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