Anilide
From Wikipedia, the free encyclopedia
In organic chemistry, anilides (or phenylamides) are a class of organic compounds with the general structure Page Module:Chem2/styles.css has no content.R−C(=O)−N(−R’)−C6H5. They are amide derivatives of aniline (Page Module:Chem2/styles.css has no content.H2N−C6H5).
Preparation
Aniline reacts with acyl chlorides or carboxylic anhydrides to give anilides. For example, reaction of aniline with acetyl chloride provides acetanilide (Page Module:Chem2/styles.css has no content.CH3−CO−NH−C6H5). At high temperatures, aniline and carboxylic acids react to give anilides.[1]
Uses
- Herbicides[2] - diflufenican, dimethenamid, flamprop, propanil, tetflupyrolimet, acetochlor, alachlor, butachlor, delachlor, diethatyl, dimethachlor, ethaprochlor, metazachlor, pretilachlor, propisochlor, pyrnachlor, terbuchlor, thenylchlor, xylachlor
- Fungicides - Oxycarboxin,[3] Carboxin[4]
References
Page Template:Reflist/styles.css has no content.
- ^ Page Module:Citation/CS1/styles.css has no content.Carl N. Webb (1941). "Benzanilide". Organic Syntheses; Page Module:Citation/CS1/styles.css has no content.Collected Volumes, vol. 1, p. 82.
- ^ Page Module:Citation/CS1/styles.css has no content."Anilide herbicides". Pesticide Target Interaction Database. East China University of Science & Technology. Archived from the original on 2018-06-24. Retrieved 2018-06-24.
- ^ Page Module:Citation/CS1/styles.css has no content.PubChem. "Oxycarboxin". PubChem. National Center for Biotechnology Information. Retrieved 2020-12-06.
- ^ Page Module:Citation/CS1/styles.css has no content.PubChem. "Carboxin". PubChem. National Center for Biotechnology Information. Retrieved 2020-12-06.
External links
- Page Template:Sister-inline/styles.css has no content.Script error: No such module "Sister project logo". Media related to Script error: No such module "Commons link". at Wikimedia Commons
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