Organoiodides
Organoiodides are a class of chemical compounds that contain an iodine atom bonded to at least one carbon atom, forming a C-I bond. These compounds play a significant role in organic synthesis and various industrial applications due to their unique reactivity and structural diversity. Organoiodides can be derived from primary, secondary, or tertiary alcohols, carboxylic acids, ketones, and other functional groups through a series of chemical transformations.
One of the key features of organoiodides is their ability to act as effective leaving groups in various organic reactions. Their reactivity makes them valuable intermediates in synthetic chemistry, enabling the construction of complex molecular structures with high precision. Additionally, organoiodides are used in polymerization processes, catalysts, and pharmaceuticals due to their specific functional properties.
In organic synthesis, organoiodides can serve as nucleophiles or electrophiles depending on the reaction conditions, allowing for a wide range of transformations such as alkylation, acylation, and arylation reactions. Their use in green chemistry initiatives is also gaining attention due to the potential for environmentally friendly processes and sustainable chemical production methods.
Overall, organoiiodides represent an important class of reagents with versatile applications across multiple fields within the chemical industry.
| 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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Kathrin Kutlescha,Rhett Kempe New J. Chem., 2010,34, 1954-1960
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Hamid Heydari,Mohammad B. Gholivand New J. Chem., 2017,41, 237-244
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Yang Chen,Di Zhou,Zheyi Meng,Jin Zhai Chem. Commun., 2016,52, 10020-10023
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Andre Prates Pereira,Tao Dong,Eric P. Knoshaug,Nick Nagle,Ryan Spiller,Bonnie Panczak,Christopher J. Chuck,Philip T. Pienkos Sustainable Energy Fuels, 2020,4, 3400-3408
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