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Crotonaldehyde
Crotonaldehyde is a chemical compound with the formula CH3CH=CHCHO. The compound is usually sold as a mixture of the E- and Z-isomers, which differ with respect to the relative position of the methyl and formyl groups. The E-isomer is more common (data given in Table is for the E-isomer). This lachrymatory liquid is moderately soluble in water and miscible in organic solvents. As an unsaturated aldehyde, crotonaldehyde is a versatile intermediate in organic synthesis. It occurs in a variety of foodstuffs, e.g. soybean oils.[1] Additional recommended knowledge
Production and usesCrotonaldehyde is produced by the aldol condensation of acetaldehyde:
Its main application is as a precursor to fine chemicals. Sorbic acid, a food preservative, and trimethylhydroquinone, a precursor to the vitamin E, are prepared from crotonaldehyde. Other derivatives include crotonic acid and 3-methoxybutanol.[1] Crotonaldehyde is a multifunctional molecule that exhibits diverse reactivity. It is an excellent prochiral dienophile.[2] It is a Michael acceptor. Addition of methylmagnesium chloride affords 3-penten-2-ol.[3] SafetyCrotonaldehyde is an irritant. It is listed as an "extremely hazardous substance" as defined by the U.S. Emergency Planning and Community Right-to-Know Act. It occurs widely in nature. See also
References
Categories: Aldehydes | Alkenes | Lachrymatory agents |
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This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "Crotonaldehyde". A list of authors is available in Wikipedia. |