Organoiodides
Organoiiodides are a class of chemical compounds characterized by the presence of an iodine atom bonded to one or more carbon atoms, typically through a C-I bond. These compounds play significant roles in organic synthesis due to their unique reactivity and stability. Organoiiodides can function as both nucleophiles and electrophiles under different reaction conditions, making them versatile tools for various chemical transformations.
One notable application of organoiiodides is their use as iodine-containing equivalents in halogenation reactions, where they replace other halogens such as bromine or chlorine in organic molecules. Organoiiodides are also employed as leaving groups in deiodination reactions and can act as protecting groups to control the reactivity of functional groups during complex synthetic pathways.
Due to their ability to facilitate efficient and selective reactions, organoiiodides have gained popularity in pharmaceuticals, agrochemicals, and materials science. Their broad use underscores the importance of these compounds in modern chemical research and industrial processes.
| Structure | Chemical Name | CAS | MF |
|---|---|---|---|
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2-iodoethan-1-amine | 52689-15-3 | C2H6IN |
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(IODOMETHYL)CYCLOPROPANE | 33574-02-6 | C4H7I |
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Iodoethane-1,1-d2 (Stabilized with Copper) | 3652-82-2 | C2H5I |
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1,1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,12,12-Pentacosafluoro-14-iodotetradecane | 30046-31-2 | C14H4F25I |
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4-iodohepta-1,6-diene | 921926-33-2 | C7H11I |
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1-Iodoheptane | 4282-40-0 | C7H15I |
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1,6-Diiodohexane | 629-09-4 | C6H12I2 |
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1-Iodooctane | 629-27-6 | C8H17I |
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1-Iodoheptafluoropropane | 754-34-7 | C3F7I |
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perfluoroheptyl iodide | 335-58-0 | C7F15I |
Related Literature
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Albertus D. Handoko,Khoong Hong Khoo,Teck Leong Tan,Hongmei Jin,Zhi Wei Seh J. Mater. Chem. A, 2018,6, 21885-21890
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Long Deng,Qian Zou,Biao Liu,Wenhui Ye,Chengfei Zhuo,Li Chen,Ze-Yuan Deng,Ya-Wei Fan,Jing Li Food Funct., 2018,9, 4234-4245
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Hanie Hashtroudi,Ian D. R. Mackinnon J. Mater. Chem. C, 2020,8, 13108-13126
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J. Xu,T. J. Carrocci,A. A. Hoskins Chem. Commun., 2016,52, 549-552
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