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Journal articles on the topic 'Trifluoromethyl-1H-pyrazole'

Author: Grafiati

Published: 4 June 2021

Last updated: 10 February 2022

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1

Palka, Barbara, Angela Di Capua, Maurizio Anzini, Gyté Vilkauskaité, Algirdas Šačkus, and Wolfgang Holzer. "Synthesis of trifluoromethyl-substituted pyrazolo[4,3-c]pyridines – sequential versus multicomponent reaction approach." Beilstein Journal of Organic Chemistry 10 (July 31, 2014): 1759–64. http://dx.doi.org/10.3762/bjoc.10.183.

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A straightforward synthesis of 6-substituted 1-phenyl-3-trifluoromethyl-1H-pyrazolo[4,3-c]pyridines and the corresponding 5-oxides is presented. Hence, microwave-assisted treatment of 5-chloro-1-phenyl-3-trifluoromethylpyrazole-4-carbaldehyde with various terminal alkynes in the presence of tert-butylamine under Sonogashira-type cross-coupling conditions affords the former title compounds in a one-pot multicomponent procedure. Oximes derived from (intermediate) 5-alkynyl-1-phenyl-3-trifluoromethyl-1H-pyrazole-4-carbaldehydes were transformed into the corresponding 1H-pyrazolo[4,3-c]pyridine 5-

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2

Fritzsche, J., M. Grzywa, D. Denysenko, et al. "CFA-14 – a perfluorinated metal–organic framework with linear 1-D CoII-chains showing temperature dependent spin-chain magnetic ordering." Dalton Transactions 47, no. 36 (2018): 12750–58. http://dx.doi.org/10.1039/c8dt02841a.

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3

AL-HILFI, Jassim Abas, Zaidoon Jawad KAHDIM, Tahseen Saddam FANDI, and Luma M. AHMED. "STRUCTURAL STUDY OF COMPLEXES FROM HEXAFLUOROACETYLACETONE, PYRAZOLE, AND ITS PYRAZOLE DERIVATIVE WITH SOME METALS BY FT-IR, AND 1H-NMR." Periódico Tchê Química 17, no. 34 (2020): 756–68. http://dx.doi.org/10.52571/ptq.v17.n34.2020.780_p34_pgs_756_768.pdf.

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The series complex formation nickel(II) or cobalt(III) with hexafluoroacetylacetone, pyrazole, 3,5-dimethylpyrazole, and 3,5-bis(trifluoromethyl)-1H-pyrazole were prepared. The first reaction step included the synthesis of the complex using hexafluoroacetylacetone as a ligand with Co(III) or Ni(II), metals with high spin with π donate and enol-form of the ligand. This formed complex was identified by FT-IR, 1H-NMR spectroscopy, and magnetic susceptibility calculation. Whereas, the second reaction step to produce the complex depended upon mixing water and pyrazole and using it as ligands with C

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4

Cheng, Long, Wen Zhao, Zhong-Hua Shen, et al. "Synthesis, Nematicidal Activity and Docking Study of Novel Pyrazole-4-Carboxamide Derivatives Against Meloidogyne incognita." Letters in Drug Design & Discovery 16, no. 1 (2018): 29–35. http://dx.doi.org/10.2174/1570180815666180326150827.

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Background:A series of novel 2,6-dichloro-4-(trifluoromethyl)phenyl)-3-(difluoromethyl)- 1H-pyrazole-4-carboxamide derivatives were designed and synthesized.Methods:All the title compounds were confirmed by 1H NMR and MS.Results and Conclusion:The primarily nematicidal activity results indicated that some of them exhibited moderate control efficacy against the tomato root-knot nematode disease caused by Meloidogyne incognita.

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5

Fritzsche, J., R. Ettlinger, M. Grzywa, et al. "CFA-15 – a perfluorinated metal–organic framework with linear 1-D CuII-chains containing accessible unsaturated, reactive metal centres." Dalton Transactions 48, no. 40 (2019): 15236–46. http://dx.doi.org/10.1039/c9dt02133g.

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The synthesis and crystal structure of the perfluorinated metal–organic framework CFA-15, CuII3(tfpc)<sub>2</sub>(OH)<sub>2</sub>·DMF, and the organic ligand H<sub>2</sub>-tfpc, 3,5-bis(trifluoromethyl)-1H-pyrazole-4-carboxylic acid, are described.

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6

Manoj Kumar, Karikere Ekanna, Parameshwar Adimoole Suchetan, Bandrehalli Siddagangaiah Palakshamurthy, Shankar Madan Kumar, Neratur Krishnappagowda Lokanath, and Swamy Sreenivasa. "5-(3,5-Difluorophenyl)-1-(4-fluorophenyl)-3-trifluoromethyl-1H-pyrazole." Acta Crystallographica Section E Structure Reports Online 70, no. 1 (2013): o19. http://dx.doi.org/10.1107/s1600536813032650.

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7

Asiri, Abdullah M., Abdulrahman O. Al-Youbi, Hassan M. Faidallah, and Seik Weng Ng. "5-Hydroxy-3-phenyl-5-trifluoromethyl-4,5-dihydro-1H-pyrazole." Acta Crystallographica Section E Structure Reports Online 67, no. 9 (2011): o2442. http://dx.doi.org/10.1107/s160053681103368x.

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8

Ghosh, S., S. Pramanik, and A. K. Mukherjee. "Structure analysis of a phenylpyrazole carboxylic acid derivative crystallizing with three molecules in the asymmetric unit (Z′ = 3) using X-ray powder diffraction." Powder Diffraction 34, no. 2 (2019): 151–58. http://dx.doi.org/10.1017/s0885715619000289.

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Crystal structure analysis of a pyrazole carboxylic acid derivative, 5-(trifluoromethyl)-1-phenyl-1H-pyrazole-4-carboxylic acid (1) has been carried out from laboratory powder X-ray diffraction data. The crystal packing in the pyrazole carboxylic acid derivative exhibits an interplay of strong O–H…O, C–H…N and C–H…F hydrogen bonds to generate a three-dimensional molecular packing via the formation ofR22(8) andR22(9) rings. Molecular electrostatic potential calculations indicated that carbonyl oxygen, pyrazole nitrogen and fluorine atoms to be the strongest acceptors. The relative contribution

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9

Park, Hyunjin, Jineun Kim, Eunjin Kwon, and Tae Ho Kim. "Crystal structure of fipronil." Acta Crystallographica Section E Crystallographic Communications 73, no. 10 (2017): 1472–74. http://dx.doi.org/10.1107/s205698901701310x.

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The title compound, C12H4Cl2F6N4OS {systematic name: 5-amino-1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-4-[(trifluoromethane)sulfinyl]-1H-pyrazole-3-carbonitrile}, is a member of the phenylpyrazole group of acaricides, and one of the phenylpyrazole group of insecticides. The dihedral angle between the planes of the pyrazole and benzene rings is 89.03 (9)°. The fluorine atoms of the trifluoromethyl substituent on the benzene ring are disordered over two sets of sites, with occupancy ratios 0.620 (15):0.380 (15). In the crystal, C—N...π interactions [N...ring centroid = 3.607 (4) Å] together wit

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10

Caruso, Francesco, Maria Valeria Raimondi, Giuseppe Daidone, Claudio Pettinari, and Miriam Rossi. "5-Amino-1-phenyl-3-trifluoromethyl-1H-pyrazole-4-carboxylic acid." Acta Crystallographica Section E Structure Reports Online 65, no. 9 (2009): o2173. http://dx.doi.org/10.1107/s1600536809032188.

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11

Spencer, Lara C., Ilia A. Guzei, Stephen O. Ojwach та James Darkwa. "trans-Bis[3,5-bis(trifluoromethyl)-1H-pyrazole-κN2]dichloropalladium(II) monohydrate". Acta Crystallographica Section C Crystal Structure Communications 62, № 9 (2006): m421—m423. http://dx.doi.org/10.1107/s0108270106025030.

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12

Jaćimović, Željko K., Sladjana B. Novaković, Goran A. Bogdanović, Milica Kosović, Eugen Libowitzky, and Gerald Giester. "Crystal structure of ethyl 3-(trifluoromethyl)-1H-pyrazole-4-carboxylate, C7H7F3N2O2." Zeitschrift für Kristallographie - New Crystal Structures 235, no. 5 (2020): 1189–90. http://dx.doi.org/10.1515/ncrs-2020-0242.

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13

Dai, Hong, Wen-Ke Miao, Shan-Shan Wu, Xue Qin, and Jian-Xin Fang. "1-Methyl-5-phenoxy-3-trifluoromethyl-1H-pyrazole-4-carbaldehyde oxime." Acta Crystallographica Section E Structure Reports Online 67, no. 4 (2011): o775. http://dx.doi.org/10.1107/s1600536811007422.

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14

Tok, Fatih, and Bedia Koçyiğit-Kaymakçıoğlu. "Design, Synthesis and Biological Screening of Novel 1,5-Diphenyl-3-(4-(trifluoromethyl)phenyl)-2-pyrazoline Derivatives." Acta Chimica Slovenica 67, no. 4 (2020): 1139–47. http://dx.doi.org/10.17344/acsi.2020.6028.

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1-Phenyl-5-substituted-3-(4-(trifluoromethyl)phenyl)-4,5-dihydro-1H-pyrazole derivatives were synthesized from chalcone derivatives. The structures of compounds were characterized by IR, 1H NMR spectroscopic methods and elemental analysis. All compounds were evaluated for their in vitro antioxidant activity using DPPH and ABTS methods, anti-inflammatory activity using lipoxygenase inhibitory method and antidiabetic activity using the α-glucosidase inhibitory method. Especially, pyrazoline derivatives exhibited stronger anti-inflammatory activity than the reference drug indomethacin (IC50: 50.4

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15

Zhang, Xiao-Hong, Jie-Zhi Chen, Ping Zhong, Hong-Ping Xiao, and Mao-Lin Hu. "1-[2,6-Dichloro-4-(trifluoromethyl)phenyl]-5-(phenylacetamido)-1H-pyrazole-3-carbonitrile." Acta Crystallographica Section E Structure Reports Online 61, no. 11 (2005): o3676—o3678. http://dx.doi.org/10.1107/s1600536805032514.

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16

Zhang, Xiao-Hong, Ping Zhong, Hong-Ping Xiao, and Mao-Lin Hu. "1-[2,6-Dichloro-4-(trifluoromethyl)phenyl]-5-(4-methoxyphenylsulfonamido)-1H-pyrazole-3-carbonitrile." Acta Crystallographica Section E Structure Reports Online 61, no. 7 (2005): o2134—o2135. http://dx.doi.org/10.1107/s160053680501812x.

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17

Zhong, Ping, Xiao-Hong Zhang, Hong-Ping Xiao, and Mao-Lin Hu. "5-(2,4-Dichlorobenzamido)-1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-1H-pyrazole-3-carbonitrile." Acta Crystallographica Section E Structure Reports Online 61, no. 10 (2005): o3110—o3111. http://dx.doi.org/10.1107/s1600536805027054.

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18

Abdul-Ghani, M., R. G. Pritchard, and A. E. Tipping. "1-Trifluoroacetyl-3-trifluoromethyl-3a,8b-dihydro-1H,4H-indeno[1,2-c]pyrazole." Acta Crystallographica Section C Crystal Structure Communications 51, no. 4 (1995): 770–72. http://dx.doi.org/10.1107/s0108270194011881.

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19

Beck, James R., and Fred L. Wright. "Synthesis of 1-aryl-5-(trifluoromethyl)-1H-pyrazole-4-carboxylic acids and esters." Journal of Heterocyclic Chemistry 24, no. 3 (1987): 739–40. http://dx.doi.org/10.1002/jhet.5570240338.

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20

Yang, Zhi-Ping, Ping Zhong, Mao-Lin Hu, Shu-Yan Li, and Ri-Yuan Tang. "1-[2,6-Dichloro-4-(trifluoromethyl)phenyl]-5-[(dimethylsulfonyl)amino]-1H-pyrazole-3-carbonitrile." Acta Crystallographica Section E Structure Reports Online 61, no. 1 (2004): o116—o117. http://dx.doi.org/10.1107/s1600536804032428.

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21

Zhang, Xiao-Hong, Ping Zhong, Zhi-Ping Yang, Mao-Lin Hu, and Hong-Ping Xiao. "5-(2-Chlorobenzamido)-1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-1H-pyrazole-3-carbonitrile." Acta Crystallographica Section E Structure Reports Online 61, no. 4 (2005): o806—o807. http://dx.doi.org/10.1107/s1600536805005763.

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22

Zhong, Ping, Xiao-Hong Zhang, Hong-Ping Xiao, and Mao-Lin Hu. "1-[2,6-Dichloro-4-(trifluoromethyl)phenyl]-5-(4-methylphenylsulfonamido)-1H-pyrazole-3-carbonitrile." Acta Crystallographica Section E Structure Reports Online 62, no. 2 (2006): o513—o515. http://dx.doi.org/10.1107/s1600536806000250.

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23

Zhang, Xing-Guo, Mu-Wang Chen, Mao-Lin Hu, and Ping Zhong. "Crystal structure of 1-(2,6-dichloro-4-(trifluoromethyl)phenyl)-5-((4-trifluoromethyl) methyleneimino)-1H-pyrazole-3-carbonitrile, C19H8Cl2F6N4." Zeitschrift für Kristallographie - New Crystal Structures 222, no. 3 (2007): 257–58. http://dx.doi.org/10.1524/ncrs.2007.0108.

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24

Li, Shu-Yan, Ping Zhong, Mao-Lin Hu, and Jin-Hai Li. "5-Amino-4-chloro-1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-1H-pyrazole-3-carbonitrile." Acta Crystallographica Section E Structure Reports Online 62, no. 7 (2006): o3090—o3091. http://dx.doi.org/10.1107/s1600536806023919.

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25

Zhong, Ping, Xiao-Hong Zhang, Zhi-Ping Yang, Hong-Ping Xiao, and Mao-Lin Hu. "1-[2,6-Dichloro-4-(trifluoromethyl)phenyl]-5-[(3,4-methylenedioxyphenyl)methyleneimino]-1H-pyrazole-3-carbonitrile." Acta Crystallographica Section E Structure Reports Online 61, no. 5 (2005): o1448—o1449. http://dx.doi.org/10.1107/s1600536805012262.

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26

Zhong, Ping, Zhiping Yang, Qian Shi, Maolin Hu, Shuyan Li, and Riyuan Tang. "1-[2,6-Dichloro-4-(trifluoromethyl)phenyl]-5-[(2-furyl)methyleneamino]-1H-pyrazole-3-carbonitrile." Acta Crystallographica Section E Structure Reports Online 61, no. 9 (2005): o2972—o2973. http://dx.doi.org/10.1107/s1600536805025699.

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27

Jiang, Ding-Xin, and Han-Hong Xu. "1-[2,6-Dichloro-4-(trifluoromethyl)phenyl]-5-iodo-4-trifluoromethylsulfinyl-1H-pyrazole-3-carbonitrile." Acta Crystallographica Section E Structure Reports Online 65, no. 8 (2009): o1774. http://dx.doi.org/10.1107/s1600536809025082.

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28

Li, Shu-Yan, Ping Zhong, Mao-Lin Hu, Yi Luo, and Jin-Hai Li. "5-[(4-Bromophenyl)methyleneimino]-1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-1H-pyrazole-3-carbonitrile." Acta Crystallographica Section E Structure Reports Online 62, no. 9 (2006): o3821—o3822. http://dx.doi.org/10.1107/s1600536806030947.

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29

Zhong, Ping, Zhiping Yang, Qian Shi, Shuyan Li, and Riyuan Tang. "1-[2,6-Dichloro-4-(trifluoromethyl)phenyl]-5-[(4-methylbenzylidene)amino]-1H-pyrazole-3-carbonitrile." Acta Crystallographica Section E Structure Reports Online 61, no. 3 (2005): o559—o560. http://dx.doi.org/10.1107/s1600536805003028.

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30

Chen, Dimei, Zhiping Yang, Ping Zhong, and Maolin Hu. "1-[2,6-Dichloro-4-(trifluoromethyl)phenyl]-5-[(4-dimethylaminobenzylidene)amino]-1H-pyrazole-3-carbonitrile." Acta Crystallographica Section E Structure Reports Online 61, no. 3 (2005): o702—o703. http://dx.doi.org/10.1107/s1600536805004654.

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31

Zhong, Ping, Zhiping Yang, and Qian Shi. "1-[2,6-Dichloro-4-(trifluoromethyl)phenyl]-5-[(4-nitrophenyl)methyleneimino]-1H-pyrazole-3-carbonitrile." Acta Crystallographica Section E Structure Reports Online 61, no. 3 (2005): o786—o787. http://dx.doi.org/10.1107/s1600536805005659.

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32

Zhang, Xiaohong, Zhiping Yang, Ping Zhong, and Maolin Hu. "1-[2,6-Dichloro-4-(trifluoromethyl)phenyl]-5-[(4-methoxyphenyl)methyleneimino]-1H-pyrazole-3-carbonitrile." Acta Crystallographica Section E Structure Reports Online 61, no. 4 (2005): o908—o909. http://dx.doi.org/10.1107/s1600536805006707.

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33

Tang, Ri-Yuan, Ping Zhong, Qiu-Lian Lin, Mao-Lin Hu, and Qian Shi. "5-Amino-1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-4-(trifluoromethylsulfanyl)-1H-pyrazole-3-carbonitrile." Acta Crystallographica Section E Structure Reports Online 61, no. 12 (2005): o4374—o4375. http://dx.doi.org/10.1107/s1600536805039280.

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34

Yang, Zhi-Ping, Ping Zhong, and Qian Shi. "1-[2,6-Dichloro-4-(trifluoromethyl)phenyl]-5-[(2-hydroxybenzylidene)amino]-1H-pyrazole-3-carbonitrile." Acta Crystallographica Section E Structure Reports Online 62, no. 2 (2006): o783—o784. http://dx.doi.org/10.1107/s1600536806002583.

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35

Li, Shu-Yan, Ping Zhong, Mao-Lin Hu, Yi Luo, and Jin-Hai Li. "5-[(2-Benzylideneethylidene)amino]-1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-1H-pyrazole-3-carbonitrile." Acta Crystallographica Section E Structure Reports Online 62, no. 6 (2006): o2333—o2334. http://dx.doi.org/10.1107/s1600536806017144.

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36

Li, Shu-Yan, Ping Zhong, and Mao-Lin Hu. "5-(3-Bromobenzylideneamino)-4-chloro-1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-1H-pyrazole-3-carbonitrile." Acta Crystallographica Section E Structure Reports Online 62, no. 7 (2006): o2832—o2833. http://dx.doi.org/10.1107/s1600536806022124.

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37

Guo, Mingliang, Kwon Ho Hong, Yongfeng Lv, et al. "A Novel and Efficient Route for Synthesis of Taladegib." Journal of Chemical Research 41, no. 2 (2017): 112–15. http://dx.doi.org/10.3184/003685017x14859543105069.

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Taladegib (LY-2940680), a small molecule Hedgehog signalling pathway inhibitor, was obtained from N-benzyl-4-piperidone via Borch reductive amination, acylation with 4-fluoro-2-(trifluoromethyl)benzoyl chloride, debenzylation, substitution with 1,4-dichlorophthalazine and Suzuki cross-coupling reaction with 1-methyl-1H-pyrazole-5-boronic acid. The advantages of this synthesis route were the elimination of Boc protection and deprotection and the inexpensive starting materials. Furthermore, the debenzylation reaction was achieved with simplified operational procedure using ammonium formate as hy

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38

Flores, Alex F. C., Bruna P. Kuhn, Darlene C. Flores, Mariano A. Pereira, Tatiane L. Balliano, and Givanildo S. da Silva. "Synthesis, Structure, and Cyclocondensation of the 4,4,4-Trifluoro-3,3-dihydroxy-2-methyl-1-(thien-2-yl)-1-butanone with Hydroxylamine and Hydrazine." Journal of Spectroscopy 2018 (2018): 1–8. http://dx.doi.org/10.1155/2018/8348652.

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The synthesis of 4,4,4-trifluoro-3,3-dihydroxy-2-methyl-1-(thien-2-yl)butan-1-one (3) through acylation of 1,1-dimethoxy-1-(thien-2-yl)propane (1) with trifluoroacetic anhydride and its reactions with hydroxylamine and hydrazine was investigated. X-ray structural analysis of new trifluoromethyl-substituted dielectrophile 3 revealed that this hydrate exists as a racemate with inter- and intramolecular O-H·O bonds. The crystal structure shows alignment along axis b of pair molecules with the same configuration of the O2-H·O1 bond. For 5(3)-trifluoromethyl-4-methyl-3(5)-(thien-2-yl)-1H-pyrazole (

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39

Yang, Zhiping, Ping Zhong, and Maolin Hu. "1-[2,6-Dichloro-4-(trifluoromethyl)phenyl]-5-(2,5-dioxo-2,5-dihydro-1H-pyrrol-1-yl)-1H-pyrazole-3-carbonitrile." Acta Crystallographica Section E Structure Reports Online 60, no. 8 (2004): o1351—o1352. http://dx.doi.org/10.1107/s1600536804016678.

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40

Hu, Huanan, Changhua Ge, Lisheng Ding, and Anjiang Zhang. "Synthesis of Novel 1-[(2,6-Dichloro-4-trifluoromethyl)phenyl]-3-aryl-1H-pyrazole-4-carbaldehydes." Molecules 15, no. 10 (2010): 7472–81. http://dx.doi.org/10.3390/molecules15107472.

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41

Xie, De-Ming, Zhan Shu, Liang Shen, Zhe-Wu Ding, and Zhi-Min Jin. "(E)-1-[2,6-Dichloro-4-(trifluoromethyl)phenyl]-5-[(dimethylamino)methyleneamino]-1H-pyrazole-4-carboxylic acid." Acta Crystallographica Section E Structure Reports Online 63, no. 12 (2007): o4562. http://dx.doi.org/10.1107/s1600536807053688.

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42

Dai, Hong, Hai-Jun Zhang, Lei Shi, Kun-Peng Luo, and Yu-Jun Shi. "1-Methyl-3-trifluoromethyl-5-[(3-chlorophenyl)sulfanyl]-1H-pyrazole-4-carbaldehydeO-(4-chlorobenzoyl)oxime." Acta Crystallographica Section E Structure Reports Online 67, no. 12 (2011): o3343. http://dx.doi.org/10.1107/s1600536811047970.

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43

Jaćimović, Željko K., Milica Kosović, Goran A. Bogdanović, Sladjana B. Novaković, Gerald Giester, and Miljan Bigović. "The crystal structure of ethyl 1-(4-nitrophenyl)-5-(trifluoromethyl)-1H-pyrazole-4-carboxylate, C13H10F3N3O4." Zeitschrift für Kristallographie - New Crystal Structures 232, no. 4 (2017): 651–53. http://dx.doi.org/10.1515/ncrs-2016-0393.

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AbstractC13H10F3N3O4, triclinic, P1̅ (no. 2), a = 7.0524(14) Å, b = 7.8044(16) Å, c = 12.954(3) Å, α = 97.93(3)°, β = 96.29(3)°, γ = 100.11(3)°, V = 688.6(3) Å3, Z = 2, Rgt(F) = 0.0478, wRref(F2) = 0.1140, T = 200 K.

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44

Yang, Zhiping, and Shuyan Li. "4-Bromo-1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-5-(4-nitrobenzylideneamino)-1H-pyrazole-3-carbonitrile." Acta Crystallographica Section E Structure Reports Online 64, no. 3 (2008): o645. http://dx.doi.org/10.1107/s160053680800545x.

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45

Zhu, Guohui, Shuyan Li, and Zhiping Yang. "4-Bromo-1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-5-(4-methoxybenzylideneamino)-1H-pyrazole-3-carbonitrile." Acta Crystallographica Section E Structure Reports Online 64, no. 3 (2008): o646. http://dx.doi.org/10.1107/s1600536808005539.

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46

Dai, Hong, Yan-Fei Shen, Jiao Chen, Hong-Lian Chen, and Yong-Jun Shen. "(E)-1-Methyl-5-(3-methyl-4-chlorophenoxy)-3-trifluoromethyl-1H-pyrazole-4-carbaldehydeO-acetyloxime." Acta Crystallographica Section E Structure Reports Online 67, no. 3 (2011): o726. http://dx.doi.org/10.1107/s1600536811006696.

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47

Yang, Zhiping, Ping Zhong, Qian Shi, Riyuan Tang, and Shuyan Li. "5-{[(4-Chlorophenyl)methylene]amino}-1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-1H-pyrazole-3-carbonitrile." Acta Crystallographica Section E Structure Reports Online 61, no. 4 (2005): o949—o950. http://dx.doi.org/10.1107/s1600536805007075.

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Liang, Ying, and Hong-Wu He. "Dimethyl [(5-chloro-1-phenyl-3-trifluoromethyl-1H-pyrazole-4-carbonyloxy)(4-methoxyphenyl)methyl]phosphonate." Acta Crystallographica Section E Structure Reports Online 62, no. 2 (2006): o485—o486. http://dx.doi.org/10.1107/s1600536806000109.

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Li, Shu-Yan, Ping Zhong, and Mao-Lin Hu. "4-Chloro-1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-5-(4-methylbenzylideneamino)-1H-pyrazole-3-carbonitrile." Acta Crystallographica Section E Structure Reports Online 62, no. 6 (2006): o2113—o2114. http://dx.doi.org/10.1107/s1600536806015157.

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Zhao, Wen, Jiahua Xing, Tianming Xu, Weili Peng, and Xinghai Liu. "Synthesis and in vivo nematocidal evaluation of novel 3-(trifluoromethyl)-1H-pyrazole-4-carboxamide derivatives." Frontiers of Chemical Science and Engineering 11, no. 3 (2016): 363–68. http://dx.doi.org/10.1007/s11705-016-1595-x.

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