N-phenylthioureas
N-Phenylthioureas are a class of organic compounds characterized by their heterocyclic structure, consisting of a benzene ring fused to a thiourea moiety. These molecules are widely used in various applications due to their diverse reactivity and structural flexibility. They serve as intermediates in the synthesis of other compounds, such as pesticides, pharmaceuticals, and dyes. Additionally, N-phenylthioureas exhibit antimicrobial properties, making them valuable for agricultural and medical applications. Their unique chemical structure endows them with potential uses in drug discovery and development, where they can act as inhibitors or modulators of biological processes. The thiourea group is particularly interesting due to its ability to form hydrogen bonds, which can contribute to the molecules' interactions with biomolecules.
| Structure | Chemical Name | CAS | MF |
|---|---|---|---|
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1,1-Diphenyl-2-thiourea | 3898-08-6 | C13H12N2S |
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1-Heptyl-3-phenyl-2-thiourea | 79425-04-0 | C14H22N2S |
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Phenylthiourea | 103-85-5 | C7H8N2S |
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1,3-bis(2-methylphenyl)thiourea | 137-97-3 | C15H16N2S |
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1-(3,4-Dichlorophenyl)thiourea | 19250-09-0 | C7H6Cl2N2S |
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1-(2,5-Dichlorophenyl)-2-thiourea | 4949-85-3 | C7H6Cl2N2S |
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1-(4-Hydroxyphenyl)thiourea | 1520-27-0 | C7H8N2OS |
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(4-methoxyphenyl)thiourea | 2293-07-4 | C8H10N2OS |
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(4-bromophenyl)thiourea | 2646-30-2 | C7H7BrN2S |
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4-Bromo-2-methylphenylthiourea | 109317-23-9 | C8H9BrN2S |
Related Literature
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Bin Han,Yasuo Shimizu,Gabriele Seguini,Celia Castro,Gérard Ben Assayag,Koji Inoue,Yasuyoshi Nagai,Sylvie Schamm-Chardon,Michele Perego RSC Adv., 2016,6, 3617-3622
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Jing Yu,Yu-Qi Lyu,Jiapeng Liu,Mohammed B. Effat,Junxiong Wu J. Mater. Chem. A, 2019,7, 17995-18002
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Dan Yang,Yanping Zhou,Xianhong Rui,Jixin Zhu,Ziyang Lu,Eileen Fong,Qingyu Yan RSC Adv., 2013,3, 14960-14962
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Zhixia Liu,Tingjian Chen,Floyd E. Romesberg Chem. Sci., 2017,8, 8179-8182
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