Acetylides
Acetylides are a class of chemical compounds characterized by the presence of an acetylidyl group (CHC≡C), which contains a triple bond between carbon atoms. These compounds are highly reactive and often unstable, making them challenging to handle and study in detail. Acetylides can be derived from the reaction of metal acetylides with alkali metals or metal carbonyls. They have applications in various fields, including organic synthesis, where they serve as precursors for synthesizing a wide range of organic compounds. Additionally, some acetylides exhibit interesting physical and chemical properties, such as luminescence under certain conditions. Due to their reactivity, careful handling is essential when working with these compounds to ensure safety and efficiency in the laboratory setting.
| Structure | Chemical Name | CAS | MF |
|---|---|---|---|
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3,4,4-trimethylpent-1-yne | 52763-16-3 | C8H14 |
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Ethenol, (2-ethynyl-2,4-cyclopentadien-1-ylidene)-, (1R)- (9CI) | 393561-91-6 | C9H6O |
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1-Eicosyne | 765-27-5 | C20H38 |
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3,3-Diethylpent-1-yne | 919-23-3 | C9H16 |
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1-Butyne, 4,4-dichloro- | 83682-42-2 | C4H4Cl2 |
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2-Methylbut-3-yn-2-amine | 2978-58-7 | C5H9N |
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pent-4-yn-1-ol | 5390-04-5 | C5H8O |
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1-Dodecyne | 765-03-7 | C12H22 |
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3-Chloro-3-methyl-1-butyne | 1111-97-3 | C5H7Cl |
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4-Methyl-1-pentyne | 7154-75-8 | C6H10 |
Related Literature
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