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Short Note


Jiangxi Provincial Key Laboratory of Functional Molecular Materials Chemistry, Faculty of Materials Metallurgy and Chemistry, Jiangxi University of Science and Technology, 86 Hongqi Road, Ganzhou 341000, China
Authors to whom correspondence should be addressed.
Molbank 2022, 2022(4), M1450;
Received: 8 August 2022 / Revised: 14 September 2022 / Accepted: 15 September 2022 / Published: 22 September 2022
(This article belongs to the Section Organic Synthesis)
This short note elaborates a concise protocol for the synthesis of 2-[difluoro(phenylselenyl)methyl]benzo-1,3-thiazole in two steps from the commercially available reagent 2-aminobenzenethiol. The structures of the synthesized compounds are confirmed by 1H-NMR, 13C-NMR and 19F-NMR spectroscopy, infrared (IR) spectra, and high-resolution mass spectrometry. View Full-Text
Keywords: 2-aminobenzenethiol; bromodifluoroacetic acid; diphenyl diselenide 2-aminobenzenethiol; bromodifluoroacetic acid; diphenyl diselenide
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MDPI and ACS Style

Xu, R.; Cai, Y.; Liao, F.; Liu, J. 2-[Difluoro(phenylselenyl)methyl]benzo-1,3-thiazole. Molbank 2022, 2022, M1450.

AMA Style

Xu R, Cai Y, Liao F, Liu J. 2-[Difluoro(phenylselenyl)methyl]benzo-1,3-thiazole. Molbank. 2022; 2022(4):M1450.

Chicago/Turabian Style

Xu, Rongfu, Ying Cai, Fumin Liao, and Jinbiao Liu. 2022. "2-[Difluoro(phenylselenyl)methyl]benzo-1,3-thiazole" Molbank 2022, no. 4: M1450.

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