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Journal articles on the topic 'Benzisothiazol'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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1

McKinnon, David M., and Kingsley R. Lee. "Fused heterocycles from o-acylbenzenethiol derivatives." Canadian Journal of Chemistry 66, no. 6 (1988): 1405–9. http://dx.doi.org/10.1139/v88-227.

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The oximes of 2-acylthioanisole derivatives may be conveniently converted into 1,2-benzisothiazoles by acetic anhydride in pyridine. 3-(2-Methylthiophenyl)-1,2-benzisothiazole, prepared by this method, has been further converted into the 1,2-benzisothiazolo[2,3-b]-1,2-benzisothiazolium system. The phenylhydrazones of certain 2-acylthioanisoles are also cyclized by polyphosphoric acid to 2-(2-methylthio)phenylindoles, which are further converted into benzo[b]thieno[3,2-b]indoles by demethylation and oxidation.

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2

McKinnon, David M., K. Ann Duncan, Aileen M. McKinnon, and Perry A. Spevack. "The preparation of some fused isothiazole derivatives." Canadian Journal of Chemistry 63, no. 4 (1985): 882–86. http://dx.doi.org/10.1139/v85-146.

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The treatment of di(2-amino-5-methylphenyl)methane with N-sulfinylmethanesulfonamide gives two materials, 3-(2-amino-5-methylphenyl)-5-methyl-2,1-benzisothiazole and what appears to be its tautomer, a 2,1-benzisothiazolo[2,3-b]-2,1-benzisothiazole derivative. Reaction of the former with methyl iodide gives mono-, di-, and trimethyl derivatives. The second of these also possesses the symmetrical 2,1-benzisothiazolo[2,3-b]-2,1-benztsothiazole structure. The structure of the other methylation product and of the acetylation products are discussed. Some 1,2-dithiol-3-ylidene-2-pyridylmethanes were

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3

Ramezanpour, Sorour, Zahra Bigdeli, Nahid Alavijeh, and Frank Rominger. "Application of Saccharin as an Acidic Partner in the Ugi Reaction for the One-Pot Synthesis of 3-Iminosaccharins." Synlett 28, no. 10 (2017): 1214–18. http://dx.doi.org/10.1055/s-0036-1558962.

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The use of saccharin as a replacement for the carboxylic acid component in an Ugi multicomponent condensation leading to [(1,1-dioxido-1,2-benzisothiazol-3-yl)amino]acetamide (3-iminosaccharin) derivatives is described for the first time.

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4

Li, Ting, Lei Yang, Kaidong Ni, Zhenyu Shi, Fei Li, and Dongyin Chen. "An efficient approach to construct benzisothiazol-3(2H)-ones via copper-catalyzed consecutive reaction of 2-halobenzamides and carbon disulfide." Organic & Biomolecular Chemistry 14, no. 26 (2016): 6297–303. http://dx.doi.org/10.1039/c6ob00819d.

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An efficient copper-catalyzed reaction for the synthesis of benzisothiazol-3(2H)-ones has been developed, starting from easily available 2-halobenzamides and carbon disulfide. The reaction proceeds via a consecutive process with S–C bond and S–N bond formation.

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5

G., S. SADANA, S. PRADHAN NITIN, and D. DEODHAR K. "Synthesis and Antibacterial Activity of 5-Arylidene-1 ,2,4-triazino [4, 3-b]-1,2-benzisothiazol- 3-one-6,6-dioxides." Journal of Indian Chemical Society Vol. 67, Oct. 1990 (1990): 861–62. https://doi.org/10.5281/zenodo.6279048.

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Department of Chemistry, G. N. Khalsa College, Bombay-400 019 Department of  Chemistry, Indian Institute of  Technology, Bombay-400 076 <em>Manuscript received </em>26 <em>September 1989, revised 16 July 1990, accepted 1 August 1990</em> Synthesis and Antibacterial Activity of  5-Arylidene-1,2,4-triazino[4,3-<em>b</em>]-1,2-benzisothiazol- 3-one-6,6-dioxides

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6

Banerjee, Bubun, Vaishali Bhardwaj, Amninder Kaur, Gurpreet Kaur, and Arvind Singh. "Catalytic Applications of Saccharin and its Derivatives in Organic Synthesis." Current Organic Chemistry 23, no. 28 (2020): 3191–205. http://dx.doi.org/10.2174/1385272823666191121144758.

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: Saccharin (1,2-benzisothiazol-3(2H)-one-1,1-dioxide) is a very mild, cheap, commercially available, water soluble, environmentally benign and edible Brønsted acidic substance. Recently, with other utilities, saccharin and its derivatives were employed as catalysts for various organic transformations. In this review, catalytic applicability of saccharin and its derivatives under various reaction conditions is summarized.

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7

Han, Hye-Jin, EunJu Kim, SunKyoung Yoo, et al. "Initial Ecological Risk Assessment of 1,2-Benzisothiazol-3-one in Environment." Journal of Korean Society of Environmental Engineers 35, no. 3 (2013): 165–70. http://dx.doi.org/10.4491/ksee.2013.35.3.165.

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8

Arshad, Muhammad Nadeem, Hafiz Mubashar-ur-Rehman, Muhammad Zia-ur-Rehman, Islam Ullah Khan, and Muhammad Shafiq. "2-(Prop-2-enyl)-1,2-benzisothiazol-3(2H)-one 1,1-dioxide." Acta Crystallographica Section E Structure Reports Online 65, no. 6 (2009): o1236. http://dx.doi.org/10.1107/s1600536809016328.

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In the title compound, C10H9NO3S, the benzisothiazole group is almost planar (with a maximum deviation of 1.61 Å). The crystal structure is stabilized by weak intermolecular C—H...O hydrogen bonds, forming a chain of molecules alongb.

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9

Kersting, Berthold. "Self-Assembly of Organo-Sulfur, Selenium and Tellurium Compounds via π-π-Stacking and Hydrogen Bonding Interactions". Zeitschrift für Naturforschung B 57, № 10 (2002): 1115–19. http://dx.doi.org/10.1515/znb-2002-1006.

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AbstractThe crystal structures of 2-isopropyl-benzisothiazol-3-one-7-carboxylicacid isopropyl amide and of the corresponding selenium and tellurium derivatives have been determined. In contrast to the sulfur and selenium compounds, the tellurium derivative has an unprecedented three-dimensional network structure held together via π-π stacking and hydrogen bonding interactions. The cavities in the 3D molecular network are filled with guestwater molecules that are hydrogen bonded to carbonyl oxygen atoms.

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10

Akpata, Ebere Immaculata, Onuabuchi Nnenna Ani, and Okwesili Fred C. Nwodo. "Phytonutrients and Anti-Nutrient Composition of Aqueous Extract of Fermented Seeds of Prosopis africana." Asian Journal of Research in Biochemistry 13, no. 3 (2023): 12–27. http://dx.doi.org/10.9734/ajrb/2023/v13i3256.

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Prosopis africana is a perennial leguminous plant in the genus Prosopis. The seeds are used as food condiment. This study was aimed at evaluating the phytochemical, proximate, vitamin and anti-nutrient compositions of aqueous extract of fermented seeds of Prosopis africana. The analyses were done using standard biochemical methods. Assessment of the bioactive constituents was carried out using gas chromatography-mass spectrometry. The result of the phytochemical analysis revealed quantifiable levels of Steroid, phenols, triterpenes, alkaloids, flavonoids, glycosides, terpenoids and saponin. Th

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11

Shah, Tariq Saeed, Waseeq Ahmad Siddiqui, M. Nawaz Tahir, and Ghulam Hussain. "N-(3-Chlorophenyl)-1,2-benzisothiazol-3-amine 1,1-dioxide." Acta Crystallographica Section E Structure Reports Online 66, no. 5 (2010): o1220. http://dx.doi.org/10.1107/s1600536810015163.

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12

Wen, Hui-Liang, Jun-Hui Zuo, Liang Ding, Bo-Wen Lai, and Chong-Bo Liu. "2-Benzyl-1,2-benzisothiazol-3(2H)-one 1,1-dioxide." Acta Crystallographica Section E Structure Reports Online 62, no. 11 (2006): o5061—o5062. http://dx.doi.org/10.1107/s160053680604116x.

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13

Siddiqui, Waseeq Ahmad, Saeed Ahmad, Hamid Latif Siddiqui, and Masood Parvez. "2-Methyl-1,2-benzisothiazol-3(2H)-one 1,1-dioxide." Acta Crystallographica Section E Structure Reports Online 64, no. 4 (2008): o724. http://dx.doi.org/10.1107/s1600536808004637.

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14

Hellwinkel, D., and R. Karle. "Ein bequemes Eintopfverfahren zur Synthese von 1,2-Benzisothiazol-1,1-dioxiden." Synthesis 1989, no. 05 (1989): 394–95. http://dx.doi.org/10.1055/s-1989-27263.

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15

Kharul, Rajendra K., Pinkal N. Prajapati, Amol A. Thorave, et al. "Effective Synthesis of 1,5-Disubstituted 2,1-Benzisothiazol-3(1H)-ones." Synthetic Communications 41, no. 22 (2011): 3265–79. http://dx.doi.org/10.1080/00397911.2010.515343.

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16

Siddiqui, Waseeq Ahmad, Saeed Ahmad, Hamid Latif Siddiqui, Rana Altaf Hussain, and Masood Parvez. "2-[(Methylsulfanyl)methyl]-1,2-benzisothiazol-3(2H)-one 1,1-dioxide." Acta Crystallographica Section E Structure Reports Online 64, no. 10 (2008): o1897. http://dx.doi.org/10.1107/s1600536808028109.

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17

Xu, Liang-Zhong, Yong-Wei Huang, Guan-Ping Yu, Pu-Yong Zhang, and Ya-Xun Yang. "2-(3,4-Dichlorobenzoylmethyl)-1,2-benzisothiazol-3(2H)-one 1,1-dioxide." Acta Crystallographica Section E Structure Reports Online 61, no. 7 (2005): o2123—o2124. http://dx.doi.org/10.1107/s1600536805018301.

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18

Wang, Limin, Xiaoyu Song, Senxiang Cheng, Tong Chen, and Deyun Cui. "Synthesis and Activity Study of 1,2-Benzisothiazol-3-one Derivatives." Chinese Journal of Organic Chemistry 44, no. 6 (2024): 1897. http://dx.doi.org/10.6023/cjoc202311021.

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19

Hu, Zhi-Qiang, Guo-Dong Si, Kai Zhou, Guan-Ping Yu, and Liang-Zhong Xu. "2-(4-Chlorobenzyl)-1,2-benzisothiazol-3(2H)-one 1,1-dioxide." Acta Crystallographica Section E Structure Reports Online 62, no. 2 (2006): o427—o428. http://dx.doi.org/10.1107/s1600536806001140.

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20

Yu, Guan-Ping, Zhong-Jie Xu, Liang-Zhong Xu, and Haji Akber Aisa. "2-n-Butyl-1,2-benzisothiazol-3(2H)-one 1,1-dioxide." Acta Crystallographica Section E Structure Reports Online 64, no. 5 (2008): o805. http://dx.doi.org/10.1107/s1600536808007733.

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21

Tari, L. W., D. M. McKinnon, and A. S. Secco. "Structure of 5-(1-methyl-2,1-benzisothiazol-3-ylideneamino)-2,4-pentadienal." Acta Crystallographica Section C Crystal Structure Communications 48, no. 4 (1992): 683–86. http://dx.doi.org/10.1107/s0108270191010570.

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22

Serebryakov, Evgeny A., Pavel G. Kislitsin, Victor V. Semenov, and Sergey G. Zlotin. "Selective Synthesis of 1,2-Benzisothiazol-3-one-1-Oxide Nitro Derivatives." Synthesis 2001, no. 11 (2001): 1659–64. http://dx.doi.org/10.1055/s-2001-16764.

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23

Li, Min, Kaili Song, Kongliang Xie, and Aiqin Hou. "Crystal morphology, dispersing stability and dyeing property of the disperse dye based on benzisothiazole." Pigment & Resin Technology 43, no. 6 (2014): 365–70. http://dx.doi.org/10.1108/prt-10-2013-0099.

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Purpose The purpose of this paper is to synthesise a disperse dye based on benzisothiazole and to characterise its crystal morphology, dispersing stability, to study the relationship between the chemical structure and the dyeing property of the dye. Design/methodology/approach The disperse dye based on benzisothiazole, 3-(3-methyl-4-N-ethyl-N-benzyl-phenyldiazenyl)-5-nitro-2,1-benzisothiazoles, was synthesized. The disperse dye based on benzisothiazole, 3-(3-methyl-4-N-ethyl-N-benzyl-phenyldiazenyl)-5-nitro-2,1-benzisothiazoles, was synthesised. The chemical structure of the dye obtained was c

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24

Takács, Eszter, Diána Lázár, Augustine Siakwa, et al. "Ecotoxicological Evaluation of Safener and Antimicrobial Additives in Isoxaflutole-Based Herbicide Formulations." Toxics 12, no. 4 (2024): 238. http://dx.doi.org/10.3390/toxics12040238.

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The environmental load by isoxaflutole and its formulated herbicide products has increasingly become apparent because, after the ban of atrazine, isoxaflutole has become its replacement active ingredient (a.i.). Obtaining information regarding the fate of this a.i. in environmental matrices and its ecotoxicological effects on aquatic organisms is essential for the risk assessment of the herbicide. In this study, the effects of Merlin Flexx- and Merlin WG75 formulated isoxaflutole-based herbicide products and two selected additives (cyprosulfamide safener and 1,2-benzisothiazol-3(2H)-one antimi

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25

BRIVIBA, Karlis, Ivan ROUSSYN, Victor S. SHAROV, and Helmut SIES. "Attenuation of oxidation and nitration reactions of peroxynitrite by selenomethionine, selenocystine and ebselen." Biochemical Journal 319, no. 1 (1996): 13–15. http://dx.doi.org/10.1042/bj3190013.

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The effect of the selenium-containing compounds selenomethionine, selenocystine and ebselen [2-phenyl-1,2-benzisoselenazol-3(2H)-one] on the oxidation of dihydrorhodamine 123 caused by peroxynitrite and on the nitration of 4-hydroxyphenylacetate by peroxynitrite was studied in comparison with their sulphur analogues methionine, cystine and ebsulfur [2-phenyl-1,2-benzisothiazol-3(2H)-one]. The selenocompounds protected dihydrorhodamine 123 from oxidation and 4-hydroxyphenylacetate from nitration more effectively than their sulphur analogues. Sodium selenite exhibited no effect. These observatio

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26

Zlotin, S. G., P. G. Kislitsin, A. I. Podgursky, et al. "Synthetic Utilization of Polynitroaromatic Compounds. 2. Synthesis of 4,6-Dinitro-1,2-benzisothiazol-3-ones and 4,6-Dinitro-1,2-benzisothiazoles from 2-Benzylthio-4,6-dinitrobenzamides." Journal of Organic Chemistry 65, no. 25 (2000): 8439–43. http://dx.doi.org/10.1021/jo000480c.

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27

Ahmad, Matloob, Hamid Latif Siddiqui, Muhammad Azam, Iftikhar Hussain Bukhari, and Masood Parvez. "2-(2-Oxo-2-phenylethyl)-1,2-benzisothiazol-3(2H)-one 1,1-dioxide." Acta Crystallographica Section E Structure Reports Online 66, no. 3 (2010): o616. http://dx.doi.org/10.1107/s1600536810005404.

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28

Akkurt, Mehmet, Şerife Pınar Yalçın, Özlen Güzel, Aydın Salman, and Orhan Büyükgüngör. "1,1,3-Trioxo-2,3-dihydro-1,2-benzisothiazol-2-ylmethyl 4-phenylpiperazine-1-carbodithioate." Acta Crystallographica Section E Structure Reports Online 63, no. 8 (2007): o3383. http://dx.doi.org/10.1107/s1600536807031595.

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29

Tyrrell, A. W. R. "Synthesis of bunte salts from 1,2-benzisothiazol-3-ones and vice versa." Tetrahedron Letters 26, no. 14 (1985): 1753–56. http://dx.doi.org/10.1016/s0040-4039(00)98330-8.

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30

Dou, Dengfeng, Deepu Alex, Bingfan Du, et al. "Antifungal activity of a series of 1,2-benzisothiazol-3(2H)-one derivatives." Bioorganic & Medicinal Chemistry 19, no. 19 (2011): 5782–87. http://dx.doi.org/10.1016/j.bmc.2011.08.029.

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31

Hanusek, Jiří, Hana Bělohlavová, Josef Přikryl, and Vladimír Macháček. "Acid-catalyzed decomposition of stable 1-(2,1-benzisothiazol-3-yl)-3-phenyltriazenes." Dyes and Pigments 80, no. 1 (2009): 136–40. http://dx.doi.org/10.1016/j.dyepig.2008.06.003.

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32

Combrink, Keith D., H. Belgin Gülgeze, Nicholas A. Meanwell, et al. "1,2-Benzisothiazol-3-one 1,1-Dioxide Inhibitors of Human Mast Cell Tryptase." Journal of Medicinal Chemistry 41, no. 24 (1998): 4854–60. http://dx.doi.org/10.1021/jm9804580.

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33

Rizzoli, Corrado, Paola Vicini, and Matteo Incerti. "4-Methyl-N-(3-oxo-2,3-dihydro-1,2-benzisothiazol-2-yl)benzenesulfonamide." Acta Crystallographica Section E Structure Reports Online 65, no. 2 (2009): o425—o426. http://dx.doi.org/10.1107/s1600536809003201.

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34

Yang, Ke, Hao Zhang, Ben Niu, Tiandi Tang, and Haibo Ge. "Benzisothiazol-3-ones through a Metal-Free Intramolecular N-S Bond Formation." European Journal of Organic Chemistry 2018, no. 40 (2018): 5520–23. http://dx.doi.org/10.1002/ejoc.201801090.

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35

Kharul, Rajendra K., Pinkal N. Prajapati, Amol A. Thorave, et al. "ChemInform Abstract: Effective Synthesis of 1,5-Disubstituted 2,1-Benzisothiazol-3(1H)-ones." ChemInform 43, no. 18 (2012): no. http://dx.doi.org/10.1002/chin.201218141.

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36

Naumov, Panče, Gligor Jovanovski, Sheng-Zhi Hu та ін. "On the short carbonyl bond in bis[μ-1,2-benzisothiazol-3(2H)-one 1,1-dioxido-κ2N:O]bis{[1,2-benzisothiazol-3(2H)-one 1,1-dioxido-κN]bis(imidazole)copper(II)}". Acta Crystallographica Section C Crystal Structure Communications 57, № 9 (2001): 1016–19. http://dx.doi.org/10.1107/s0108270101009507.

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37

Betari, Nibal, Kristoffer Sahlholm, Yuta Ishizuka, Knut Teigen, and Jan Haavik. "Discovery and biological characterization of a novel scaffold for potent inhibitors of peripheral serotonin synthesis." Future Medicinal Chemistry 12, no. 16 (2020): 1461–74. http://dx.doi.org/10.4155/fmc-2020-0127.

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Aim: Tryptophan hydroxylase 1 (TPH1) catalyzes serotonin synthesis in peripheral tissues. Selective TPH1 inhibitors may be useful for treating disorders related to serotonin dysregulation. Results & methodology: Screening using a thermal shift assay for TPH1 binders yielded Compound 1 (2-(4-methylphenyl)-1,2-benzisothiazol-3(2 H)-one), which showed high potency (50% inhibition at 98 ± 30 nM) and selectivity for inhibiting TPH over related aromatic amino acid hydroxylases in enzyme activity assays. Structure–activity relationships studies revealed several analogs of 1 showing comparable pot

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38

Niu, Zhihao, Qiaozhuo Wu, Qingzhong Li, and Steve Scheiner. "C∙∙∙O and Si∙∙∙O Tetrel Bonds: Substituent Effects and Transfer of the SiF3 Group." International Journal of Molecular Sciences 24, no. 15 (2023): 11884. http://dx.doi.org/10.3390/ijms241511884.

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The tetrel bond (TB) between 1,2-benzisothiazol-3-one-2-TF3-1,1-dioxide (T = C, Si) and the O atom of pyridine-1-oxide (PO) and its derivatives (PO-X, X = H, NO2, CN, F, CH3, OH, OCH3, NH2, and Li) is examined by quantum chemical means. The Si∙∙∙O TB is quite strong, with interaction energies approaching a maximum of nearly 70 kcal/mol, while the C∙∙∙O TB is an order of magnitude weaker, with interaction energies between 2.0 and 2.6 kcal/mol. An electron-withdrawing substituent on the Lewis base weakens this TB, while an electron-donating group has the opposite effect. The SiF3 group transfers

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39

Zhong, Qihao, Zhiqiang Xiong, Shouri Sheng, and Junmin Chen. "Electrochemical synthesis for benzisothiazol-3(2H)-ones by dehydrogenative N S bond formation." Tetrahedron Letters 80 (September 2021): 153323. http://dx.doi.org/10.1016/j.tetlet.2021.153323.

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40

Khalid, Zunera, Hamid Latif Siddiqui, Matloob Ahmad, Iftikhar Hussain Bukhari, and Masood Parvez. "2-[2-(3-Chlorophenyl)-2-oxoethyl]-1,2-benzisothiazol-3(2H)-one 1,1-dioxide." Acta Crystallographica Section E Structure Reports Online 66, no. 3 (2010): o617. http://dx.doi.org/10.1107/s1600536810005428.

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41

Gul, Salman, Hamid Latif Siddiqui, Matloob Ahmad, Muhammad Azam, and Masood Parvez. "2-[2-(3-Methoxyphenyl)-2-oxoethyl]-1,2-benzisothiazol-3(2H)-one 1,1-dioxide." Acta Crystallographica Section E Structure Reports Online 66, no. 3 (2010): o618. http://dx.doi.org/10.1107/s160053681000543x.

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42

Arshad, Muhammad Nadeem, Hafiz Mubashar-ur-Rehman, Muhammad Zia-ur-Rehman, Islam Ullah Khan, and Muhammad Shafique. "2-[(E)-3-Phenylprop-2-enyl]-1,2-benzisothiazol-3(2H)-one 1,1-dioxide." Acta Crystallographica Section E Structure Reports Online 65, no. 5 (2009): o1011. http://dx.doi.org/10.1107/s1600536809012999.

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43

Ng, S. W. "2-Triphenylstannyl-1,2-benzisothiazol-3(2H)-one 1,1-Dioxide–Triphenylphosphine Oxide (1/1)." Acta Crystallographica Section C Crystal Structure Communications 52, no. 6 (1996): 1365–67. http://dx.doi.org/10.1107/s0108270196001898.

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44

Kamigata, Nobumasa, Hirokazu Iizuka, and Michio Kobayashi. "Photochemical Isomerization of 2-Pyridyl- and 2-Pyrazinyl-1,2-benzisothiazol-3(2H)-ones." Bulletin of the Chemical Society of Japan 59, no. 5 (1986): 1601–2. http://dx.doi.org/10.1246/bcsj.59.1601.

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45

Carmellino, ML, G. Pagani, M. Pregnolato, M. Terreni, and F. Pastoni. "Antimicrobial activity of fluorinated 1,2-benzisothiazol-3(2H)-ones and 2,2′-dithiobis(benzamides)." European Journal of Medicinal Chemistry 29, no. 10 (1994): 743–51. http://dx.doi.org/10.1016/0223-5234(94)90132-5.

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46

Serebryakov, Evgeny A., Pavel G. Kislitsin, Victor V. Semenov, and Sergey G. Zlotin. "ChemInform Abstract: Selective Synthesis of 1,2-Benzisothiazol-3-one-1-oxide Nitro Derivatives." ChemInform 33, no. 4 (2010): no. http://dx.doi.org/10.1002/chin.200204154.

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47

Mckinnon, David M., and K. Ann Duncan. "The 2,1-benzisothiazolo[2,3-b]-2,1-benzisothiazole system, synthesis and properties." Journal of Heterocyclic Chemistry 25, no. 4 (1988): 1095–98. http://dx.doi.org/10.1002/jhet.5570250409.

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48

Zlotin, S. G., P. G. Kislitsin, A. I. Podgursky, et al. "ChemInform Abstract: Synthetic Utilization of Polynitroaromatic Compounds. Part 2. Synthesis of 4,6-Dinitro-1,2-benzisothiazol-3-ones and 4,6-Dinitro-1,2-benzisothiazoles from 2-Benzylthio-4,6-dinitrobenzamides." ChemInform 32, no. 17 (2001): no. http://dx.doi.org/10.1002/chin.200117089.

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Liu, Dongdong, Miao Dong, Jianxin Yang, and Qiang Lin. "Performance of Marine Bioactivities of N-Acyloxyethyl-1,2-Benzisothiazol-3(2H)-one Antifouling Paint." IOP Conference Series: Materials Science and Engineering 382 (July 2018): 022011. http://dx.doi.org/10.1088/1757-899x/382/2/022011.

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Arshad, Muhammad Nadeem, M. Nawaz Tahir, Islam Ullah Khan, Muhammad Humayun Bilal, and Hafiz Mubashar-ur-Rehman. "2-(3-Methylbut-2-en-1-yl)-1,2-benzisothiazol-3(2H)-one 1,1-dioxide." Acta Crystallographica Section E Structure Reports Online 65, no. 5 (2009): o986. http://dx.doi.org/10.1107/s1600536809012021.

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