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Journal articles on the topic '(dichloro-2'

Author: Grafiati

Published: 4 June 2021

Last updated: 10 February 2022

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1

Britton, D. "4,5-Dichloro-2-nitroaniline." Acta Crystallographica Section C Crystal Structure Communications 55, no. 10 (1999): IUC9900116. http://dx.doi.org/10.1107/s0108270199098698.

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2

Fan, Ying, Wei You, Jian-Lan Liu, Hui-Fen Qian, and Wei Huang. "3,5-Dichloro-2-hydroxybenzaldehyde." Acta Crystallographica Section E Structure Reports Online 64, no. 6 (2008): o1080. http://dx.doi.org/10.1107/s1600536808013901.

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3

Ourari, Ali, Lotfi Baameur, Sofiane Bouacida, Bouet Gilles, and Allain Magali. "2,4-Dichloro-6-({2-[(3,5-dichloro-2-hydroxybenzylidene)amino]ethyl}iminomethyl)phenol." Acta Crystallographica Section E Structure Reports Online 68, no. 6 (2012): o1700. http://dx.doi.org/10.1107/s1600536812020235.

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The title molecule, C16H12Cl4N2O2, lies about an inversion center. The symmetry-unique part of the molecule contains an intramolecular O—H...N hydrogen bond. In the crystal, molecules are arranged in corrugated layers parallel to (-101). Weak π–π stacking interactions, with a centroid–centroid diatance of 3.7923 (13) Å, are present.

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4

Kia, Reza, Hadi Kargar, Amir Adabi Ardakani, and Muhammad Nawaz Tahir. "4,6-Dichloro-2-[(E)-(2-{[(E)-3,5-dichloro-2-oxidobenzylidene]azaniumyl}ethyl)iminiumylmethyl]phenolate." Acta Crystallographica Section E Structure Reports Online 68, no. 7 (2012): o2242—o2243. http://dx.doi.org/10.1107/s160053681202870x.

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5

Li, Wen-Hui. "2′-(3,5-Dichloro-2-hydroxybenzylidene)-2-hydroxybenzohydrazide." Acta Crystallographica Section E Structure Reports Online 63, no. 5 (2007): o2136—o2137. http://dx.doi.org/10.1107/s1600536807014195.

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6

Kiwan, A. Mageed, Fatma Hayder, and Fathy Hassan. "Studies on 3,3′-dichloro-, 4,4′-dichloro- and 5,5′-dichloro,2-2′-dimethyldithizone and their reactions with metal ions." Analytica Chimica Acta 182 (1986): 245–50. http://dx.doi.org/10.1016/s0003-2670(00)82458-7.

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7

Kargar, Hadi, Reza Kia, Amir Adabi Ardakani, and Muhammad Nawaz Tahir. "4,6-Dichloro-2-((E)-{4-[(E)-3,5-dichloro-2-hydroxybenzylideneamino]butylimino}methyl)phenol." Acta Crystallographica Section E Structure Reports Online 68, no. 7 (2012): o2244—o2245. http://dx.doi.org/10.1107/s1600536812028693.

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8

You, Zhong-Lu. "Dichloro{2,4-dichloro-6-[2-(dimethylamino)ethyliminomethyl]phenolato}zinc(II)." Acta Crystallographica Section E Structure Reports Online 61, no. 11 (2005): m2416—m2418. http://dx.doi.org/10.1107/s1600536805034744.

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9

Hu, Yang-Jian. "Dichloro{2,4-dichloro-6-[2-(isopropylammonio)ethyliminomethyl]phenolato}zinc(II)." Acta Crystallographica Section E Structure Reports Online 62, no. 10 (2006): m2515—m2516. http://dx.doi.org/10.1107/s1600536806035458.

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10

Lynch, Daniel E., and Ian McClenaghan. "4,6-Dichloro-2-(methylthio)pyrimidine." Acta Crystallographica Section C Crystal Structure Communications 56, no. 11 (2000): e536-e536. http://dx.doi.org/10.1107/s0108270100014190.

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11

Janczak, Jan, and Ryszard Kubiak. "Two isomorphous complexes: dichloro[phthalocyaninato(2–)]tin(IV) and dichloro[phthalocyaninato(2–)]germanium(IV)." Acta Crystallographica Section C Crystal Structure Communications 59, no. 6 (2003): m237—m240. http://dx.doi.org/10.1107/s0108270103009417.

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12

Ajiboye, TO, RA Ajala-Lawal, and AB Adeyiga. "Caffeic acid abrogates 1,3-dichloro-2-propanol-induced hepatotoxicity by upregulating nuclear erythroid-related factor 2 and downregulating nuclear factor-kappa B." Human & Experimental Toxicology 38, no. 9 (2019): 1092–101. http://dx.doi.org/10.1177/0960327119851257.

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1,3-dichloro-2-propanol is a food-borne contaminant reported to cause liver injury. In this study, we evaluated the protective influence of caffeic acid on 1,3-dichloro-2-propanol-induced hepatotoxicity in rats. Rats were randomized into five groups (A–E). Rats received distilled water or caffeic acid (10 or 20 mg/kg body weight) for 7 days. In addition, rats were challenged with 1,3-dichloro-2-propanol on day 7. Caffeic acid prevented 1,3-dichloro-2-propanol-mediated alterations in alkaline phosphatase, alanine and aspartate aminotransferases, albumin and total bilirubin in the serum of rats.

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13

Mistry, Rakesh N., and K. R. Desai. "Studies on Synthesis of Some Novel Heterocyclic Chalcone, Pyrazoline, Pyrimidine - 2 - One, Pyrimidine - 2 - Thione,para-Acetanilide Sulphonyl and Benzoyl Derivatives and their Antimicrobial Activity." E-Journal of Chemistry 2, no. 1 (2005): 30–41. http://dx.doi.org/10.1155/2005/953107.

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1, 2 - Dichloro benzene on chlorosulphonation by chlorosulphonic acid gives 1, 2 - [dichloro] - benzene sulphonyl chloride which on condensation withp–amino acetophenone gives 1-[acetyl] - 1’ , 2’ - [dichloro] - dibenz sulphonamide derivative. This derivative undergo condensation with 2,4- dichloro benzaldehyde gives 1- [3” - (sub. phenyl) - 2” - propene - 1” - one] - 1’ , 2’ - [dichloro] - dibenz sulphonamide derivative which on reaction with 99% hydrazine hydrate and glacial acetic acid gives 1-[acetyl]-3- [1’ , 2’ - (dichloro) - dibenz sulphonamide] -5 - [2” , 4” - dichloro phenyl] - 2 - py

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14

Saluja, Sunita, Ruiming Zou, John C. Drach, and Leroy B. Townsend. "Structure−Activity Relationships among 2-Substituted 5,6-Dichloro-, 4,6-Dichloro-, and 4,5-Dichloro-1-[(2-hydroxyethoxy)methyl]- and -1-[(1,3-dihydroxy-2-propoxy)methyl]benzimidazoles." Journal of Medicinal Chemistry 39, no. 4 (1996): 881–91. http://dx.doi.org/10.1021/jm950556a.

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15

Li, Xiao-Yan. "(E)-N′-(3,5-Dichloro-2-hydroxybenzylidene)-2-methoxybenzohydrazide." Acta Crystallographica Section E Structure Reports Online 67, no. 7 (2011): o1798. http://dx.doi.org/10.1107/s160053681102366x.

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16

Büyükgüngör, Orhan, and Mustafa Odabaşoğlu. "5,6-Dichloro-2-(2-hydroxyphenyl)isoindoline-1,3-dione." Acta Crystallographica Section E Structure Reports Online 64, no. 5 (2008): o778. http://dx.doi.org/10.1107/s1600536808008180.

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17

Büyükgüngör, Orhan, and Mustafa Odabaşoğlu. "5,6-Dichloro-2-(2-fluorophenyl)isoindoline-1,3-dione." Acta Crystallographica Section E Structure Reports Online 64, no. 5 (2008): o882. http://dx.doi.org/10.1107/s1600536808010544.

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18

Peng, San-Jun, Cong-Shan Zhou, and Tao Yang. "Dichloro{2-[2-(ethylamino)ethyliminomethyl]phenolato}zinc(II)." Acta Crystallographica Section E Structure Reports Online 62, no. 5 (2006): m1147—m1149. http://dx.doi.org/10.1107/s1600536806014759.

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In the title mononuclear zinc(II) complex, [ZnCl2(C11H16N2O)], the ZnII atom is coordinated by the imine N and phenolate O atoms of the Schiff base ligand and two chloride anions to give a four-coordinate tetrahedral geometry. In the crystal structure, the molecules are linked through intermolecular N—H...O, N—H...Cl and C—H...Cl hydrogen bonds, forming layers parallel to the ab plane.

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19

Peters, A. "Hetarylazo disperse dyes derived from 5,6-dichloro-and 6,7-dichloro-2 aminobenzothiazoles." Dyes and Pigments 20, no. 1 (1992): 41–51. http://dx.doi.org/10.1016/0143-7208(92)80039-p.

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20

Lynch, Daniel E., and Ian McClenaghan. "4,6-Dichloro-2-methylthio-5-phenylpyrimidine." Acta Crystallographica Section E Structure Reports Online 57, no. 3 (2001): o264—o265. http://dx.doi.org/10.1107/s1600536801003154.

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21

Kabak, M., Y. Elerman, V. Güner, S. Yildirir, and T. N. Durlu. "3,3-Dichloro-1,4-diphenylazetidin-2-one." Acta Crystallographica Section C Crystal Structure Communications 55, no. 9 (1999): 1511–12. http://dx.doi.org/10.1107/s0108270199006095.

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22

Resinger, Ales, Curt Wentrup, Karl A. Byriel, and Colin H. L. Kennard. "N-(3,5-Dichloro-2-pyridyl)formamide." Acta Crystallographica Section E Structure Reports Online 61, no. 7 (2005): o2053—o2054. http://dx.doi.org/10.1107/s1600536805017605.

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23

Pinkus, A. G., Kevin K. Klausmeyer, Rodney P. Feazell, Ching T. Wang, and Charles G. Moseley. "2-[Dichloro(phenoxy)methyl]phenyl dichlorophosphonate." Acta Crystallographica Section E Structure Reports Online 60, no. 8 (2004): o1312—o1313. http://dx.doi.org/10.1107/s1600536804016290.

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24

Arun Prasad, M., Babu Varghese, and M. V. Sangaranarayanan. "5-Bromo-1,3-dichloro-2-iodobenzene." Acta Crystallographica Section E Structure Reports Online 60, no. 11 (2004): o1933—o1934. http://dx.doi.org/10.1107/s160053680402392x.

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25

Gowda, B. Thimme, Sabine Foro, P. G. Nirmala, and Hartmut Fuess. "2,4-Dichloro-N-(2-chlorophenyl)benzenesulfonamide." Acta Crystallographica Section E Structure Reports Online 66, no. 7 (2010): o1641. http://dx.doi.org/10.1107/s1600536810021306.

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26

Fun, Hoong-Kun, Reza Kia, Annada C. Maity, Sibaprasad Maity, and Shyamaprosad Goswami. "3,5-Dichloro-6-methylpyridin-2-amine." Acta Crystallographica Section E Structure Reports Online 65, no. 1 (2008): o97. http://dx.doi.org/10.1107/s1600536808041366.

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27

Gowda, B. Thimme, Sabine Foro, P. G. Nirmala, and Hartmut Fuess. "2,4-Dichloro-N-(2-methylphenyl)benzenesulfonamide." Acta Crystallographica Section E Structure Reports Online 66, no. 10 (2010): o2542. http://dx.doi.org/10.1107/s1600536810035166.

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28

Kargar, Hadi, Reza Kia, Saeideh Abbasian, and Muhammad Nawaz Tahir. "4,6-Dichloro-2-{[(E)-(3-{[(E)-3,5-dichloro-2-hydroxybenzylidene]amino}-2,2-dimethylpropyl)imino]methyl}phenol." Acta Crystallographica Section E Structure Reports Online 68, no. 1 (2011): o142. http://dx.doi.org/10.1107/s1600536811053438.

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29

Lee, Sung Jea, Jun Yong Lee, Hyun Woong Yang, Cheal Kim, Wonwoo Nam, and Youngmee Kim. "Tetraethylammonium dichloro[4,5-dichloro-1,2-bis(2-pyridine-2-carboxamido)benzene]ferrate(III), [Et4N][(bpc)FeCl2]." Acta Crystallographica Section E Structure Reports Online 58, no. 6 (2002): m313—m315. http://dx.doi.org/10.1107/s1600536802009273.

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30

Jeong, Ji-Hak, Ik-Jae Sin, Yeong-Min Sin, Heung-Jai Park, and Won-Gun An. "1,3-Dichloro-2-Propanol (1,3-DCP) Induced Cell Damage." Journal of Environmental Science International 16, no. 2 (2007): 219–25. http://dx.doi.org/10.5322/jes.2007.16.2.219.

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31

Gowda, Basavalinganadoddy Thimme, Helmut Paulus, and Jozef Kožíšek. "Effect of Substitution on the Molecular Geometry of N-(2/3/4-Substituted-phenyl)-2,2-dichloro-acetamides, 2/3/4-XC6H4NH-CO-CHCl2 (X = CH3 or Cl)." Zeitschrift für Naturforschung A 61, no. 12 (2006): 675–82. http://dx.doi.org/10.1515/zna-2006-1210.

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2MPDCAThe effect of ring substitution on the molecular geometry of amides of the type 2/3/4-XC6H4NHCO- CHCl2 (X = CH3 or Cl) has been studied by determining the crystal structures of the compounds N-(2-methylphenyl)-2,2-dichloro-acetamide, 2-CH3C6H4NH-CO-CHCl2 (); N-(3-methylphenyl)- 2,2-dichloro-acetamide, 3-CH3C6H4NH-CO-CHCl2 (3MPDCA) and N-(3-chlorophenyl)- 2,2-dichloro-acetamide, 3-ClC6H4NH-CO-CHCl2 (3CPDCA). The results are analyzed along with our earlier crystal structures of the amides N-(phenyl)-2,2-dichloro-acetamide, C6H5NH-COCHCl2 (PDCA); N-chloro-N-(phenyl)-2,2-dichloro-acetamide,

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32

Dumdei, Eric J., Jamie S. Simpson, Mary J. Garson, Karl A. Byriel, and Colin H. L. Kennard. "New Chlorinated Metabolites from the Tropical Marine Sponge Dysidea herbacea." Australian Journal of Chemistry 50, no. 2 (1997): 139. http://dx.doi.org/10.1071/c96111.

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Three new chlorinated metabolites, namely 3-(3,3-dichloro-2-methylpropyl)-6-(3,3-dichloro-2-methyl-propylidene)-1,4-dimethylpiperazine-2,5-dione (3), 1-methyl-3-(3,3,3-trichloro-2-methylpropyl)-6-(3,3,3-richloro-2-methylpropylidene)piperazine-2,5-dione (4) and 5,5-dichloro-4-methyl-2-[methyl(4,4-dichloro-3-methyl-1-oxobutyl)amino]-N-(thiazol-2-ylmethyl)pentanamide (8), have been isolated from collections of Dysidea herbacea from the southern region of the Great Barrier Reef. The relative and absolute stereochemistry of (4) was determined by X-ray crystallographic analysis.

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33

Pollmann, Katrin, Stefan Kaschabek, Victor Wray, Walter Reineke, and Dietmar H. Pieper. "Metabolism of Dichloromethylcatechols as Central Intermediates in the Degradation of Dichlorotoluenes by Ralstonia sp. Strain PS12." Journal of Bacteriology 184, no. 19 (2002): 5261–74. http://dx.doi.org/10.1128/jb.184.19.5261-5274.2002.

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ABSTRACT Ralstonia sp. strain PS12 is able to use 2,4-, 2,5-, and 3,4-dichlorotoluene as growth substrates. Dichloromethylcatechols are central intermediates that are formed by TecA tetrachlorobenzene dioxygenase-mediated activation at two adjacent unsubstituted carbon atoms followed by TecB chlorobenzene dihydrodiol dehydrogenase-catalyzed rearomatization and then are channeled into a chlorocatechol ortho cleavage pathway involving a chlorocatechol 1,2-dioxygenase, chloromuconate cycloisomerase, and dienelactone hydrolase. However, completely different metabolic routes were observed for the t

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34

Cantillana, Tatiana, and Lars Eriksson. "(2S)-1,1-Dichloro-2-(2-chlorophenyl)-2-(4-chlorophenyl)ethane." Acta Crystallographica Section E Structure Reports Online 65, no. 2 (2009): o297. http://dx.doi.org/10.1107/s160053680804405x.

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35

Arora, Pankaj Kumar, Mi-Jeong Jeong, and Hanhong Bae. "Chemotaxis Away from 4-Chloro-2-nitrophenol, 4-Nitrophenol, and 2,6-Dichloro-4-nitrophenol byBacillus subtilisPA-2." Journal of Chemistry 2015 (2015): 1–4. http://dx.doi.org/10.1155/2015/296231.

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Bacterial strain PA-2 exhibits chemotaxis away from 4-chloro-2-nitrophenol, 4-nitrophenol, and 2,6-dichloro-4-nitrophenol. This strain was identified asBacillus subtilison the basis of the 16S rRNA gene sequencing. The drop plate assay and the chemical-in-plug method were used to demonstrate negative chemotactic behavior of strain PA-2. The growth studies showed that strain PA-2 did not utilize 4-chloro-2-nitrophenol, 4-nitrophenol, and 2,6-dichloro-4-nitrophenol as its sole sources of carbon and energy. This is the first report of negative chemotaxis of 4-chloro-2-nitrophenol, 4-nitrophenol,

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36

Usman, Anwar, Hoong-Kun Fun, Suchada Chantrapromma, Hai-Liang Zhu, and Qiong-Xin Liu. "Dichloro{2-[N-(2-hydroxyethylammonioethyl)iminomethyl]phenolate}zinc(II)." Acta Crystallographica Section E Structure Reports Online 59, no. 2 (2003): o215—o217. http://dx.doi.org/10.1107/s1600536803001144.

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37

Chandia, N. P., J. C. Canales, I. Azocar, et al. "Synthesis of 5,5′-Dialkyl-6,6′-dichloro-2, 2′-bipyridines." Synthetic Communications 39, no. 5 (2009): 927–39. http://dx.doi.org/10.1080/00397910802440348.

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38

Vilela, Sérgio M. F., Filipe A. Almeida Paz, João P. C. Tomé, Verónica de Zea Bermudez, José A. S. Cavaleiro, and João Rocha. "Methyl 2-(4,6-dichloro-1,3,5-triazin-2-ylamino)acetate." Acta Crystallographica Section E Structure Reports Online 65, no. 8 (2009): o1985—o1986. http://dx.doi.org/10.1107/s1600536809028670.

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39

Yang, De-Suo, and Jin-Bao Guo. "2′-[1-(3,5-Dichloro-2-hydroxyphenyl)methylidene]isonicotinohydrazide monohydrate." Acta Crystallographica Section E Structure Reports Online 62, no. 10 (2006): o4414—o4415. http://dx.doi.org/10.1107/s1600536806035811.

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40

Qiu, Xiao-Yang. "Dichloro{2-[2-(ethylamino)ethyliminomethyl]-4-nitrophenolato}zinc(II)." Acta Crystallographica Section E Structure Reports Online 62, no. 9 (2006): m2175—m2176. http://dx.doi.org/10.1107/s1600536806031461.

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41

Husson, Jérôme, and Laurent Guyard. "4,4″-Dichloro-4′-(2-thienyl)-2,2′:6′,2″-terpyridine." Molbank 2019, no. 3 (2019): M1071. http://dx.doi.org/10.3390/m1071.

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A new thiophene-substituted terpyridine derivative has been prepared and characterized. This ligand features a thiophene heterocycle (as an electrochemically polymerizable unit) as well as two chlorine atoms for further functionalization.

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42

Du, Gui-Xiang, Jun Li та Feng-Xing Zhang. "Dichloro[2-(2-furyl)-1H-benzimidazole-κN3]copper(II)". Acta Crystallographica Section E Structure Reports Online 61, № 1 (2004): m119—m120. http://dx.doi.org/10.1107/s1600536804031009.

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43

Wang, Shou-Xing. "Dichloro{2-[(2-isopropylaminoethylimino)methyl]-4-nitrophenolato}zinc(II)." Acta Crystallographica Section E Structure Reports Online 63, no. 3 (2007): m706—m707. http://dx.doi.org/10.1107/s1600536807006010.

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In the title compound, [ZnCl2(C12H17N3O3)], a mononuclear Schiff base zinc(II) complex, the Zn atom is tetrahedrally coordinated by one imine N atom and one phenolate O-atom of the Schiff base ligand and by two terminal chloride anions. In the crystal structure, symmetry-related molecules are linked through intermolecular N—H...Cl, N—H...O and C—H...Cl hydrogen bonds, forming chains running parallel to the b axis.

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44

Koopman, H., J. H. Uhlenbroek, H. H. Haeck, J. Daams, and M. J. Koopmans. "Investigations on herbicides II: 2-Alkyloxy- and 2-aryloxy -4,6-dichloro-1,3,5-triazines 2-Alkylthio- and 2-arylthio-4,6-dichloro-1,3,5-triazines." Recueil des Travaux Chimiques des Pays-Bas 78, no. 12 (2010): 967–80. http://dx.doi.org/10.1002/recl.19590781205.

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45

Mistry, Bhavnaben D., Kishor R. Desai, and Nigam J. Desai. "SYNTHESIS, IN VITRO ANTIMICROBIAL ACTIVITY OF SCHIFF’S BASE, AZETIDINONES AND THIAZOLIDINONES." International Journal of Current Pharmaceutical Research 9, no. 1 (2016): 126. http://dx.doi.org/10.22159/ijcpr.2017v9i1.16634.

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Objective: The objective of the present study is to synthesize 3-Chloro-4-[3-(2,4-dichloro-5-fluoro phenyl)-1H-pyrazol-4-yl]-1-(substituted) azetidin-2-one [4a-n] and 2-[3-(2,4-Dichloro-5-fluoro phenyl)-1H-pyraol-4-yl]-3-(substituted phenyl)-1,3-thiazolidin-4-one [5a-n]. The structure of all synthesized compounds were characterized by IR, 1H NMR, 13C NMR and mass spectral studies. Methods: The titled compounds 3-Chloro-4-[3-(2,4-dichloro-5-fluoro phenyl)-1H-pyrazol-4-yl]-1-(substituted) azetidin-2-one [4a-n] and 2-[3-(2,4-Dichloro-5-fluoro phenyl)-1H-pyraol-4-yl]-3-(substituted phenyl)-1,3-thi

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46

Elix, John A., Caroline E. Barclay,, H. Thorsten Lumbsch, and Judith H. Wardlaw. "New Chloro Depsides from the Lichen Lecanora lividocinerea." Australian Journal of Chemistry 50, no. 10 (1997): 971. http://dx.doi.org/10.1071/c97052.

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The new depsides 3,5-dichloro-2′-O-methylnorstenosporic acid (4), 5-chloro-2′-O-methylanziaic acid (5) and 3,5-dichloro-2′-O-methylnorhyperlatolic acid (6) have been detected in the lichenLecanora lividocinerea and the structures of these metabolites have been established by unambiguous synthesis. In addition, the synthesis of the depside 3,5-dichloro-4-O-demethylplanaic acid (7) is described.

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47

Moncol, Ján, Klaudia Jomová, and Mária Porubská. "Two centrosymmetric dinuclear phenanthroline–copper(II) complexes with 3,5-dichloro-2-hydroxybenzoic acid and 5-chloro-2-hydroxybenzoic acid." Acta Crystallographica Section C Crystal Structure Communications 68, no. 4 (2012): m85—m89. http://dx.doi.org/10.1107/s0108270112004532.

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The title compounds, bis(μ-3,5-dichloro-2-oxidobenzoato)-κ3O1,O2:O2;κ3O2:O1,O2-bis[(3,5-dichloro-2-hydroxybenzoic acid-κO1)(1,10-phenanthroline-κ2N,N′)copper(II)], [Cu2(C7H2Cl2O3)2(C7H4Cl2O3)2(C12H8N2)2], (I), and bis(μ-5-chloro-2-oxidobenzoato)-κ3O1,O2:O1;κ3O1:O1,O2-bis[(5-chloro-2-hydroxybenzoic acid-κO1)(1,10-phenanthroline-κ2N,N′)copper(II)] ethanol monosolvate, [Cu2(C7H3ClO3)2(C7H5ClO3)2(C12H8N2)2]·C2H6O, (II), contain centrosymmetric dinuclear complex molecules in which Cu2+cations are surrounded by a chelating 1,10-phenanthroline ligand, a chelating 3,5-dichloro-2-oxidobenzoate or 5-chl

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Wilhelm, P., C. Boss, M. Pfammatter, et al. "(4,6-Dichloro-1,3,5-triazin-2-ylethynyl)dimethylamine." Acta Crystallographica Section C Crystal Structure Communications 52, no. 8 (1996): 2004–6. http://dx.doi.org/10.1107/s0108270196002545.

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Barnett, Sarah A., Andrea Johnston, Alastair J. Florence, and Alan R. Kennedy. "3,4-Dichloro-1-nitrobenzene–aniline (2/1)." Acta Crystallographica Section E Structure Reports Online 61, no. 7 (2005): o2318—o2319. http://dx.doi.org/10.1107/s1600536805019999.

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Ren, Tian-tian, Zhong Zhang, Cong-cong Zhong, Zhong-zhi Yang, and Zhan-wang Shi. "4,6-Dichloro-5-(2-methoxyphenoxy)-2,2′-bipyrimidine." Acta Crystallographica Section E Structure Reports Online 67, no. 6 (2011): o1334. http://dx.doi.org/10.1107/s160053681101419x.

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