Chemistry:Anilide
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Short description: Organic compounds of the form RC(=O)N(R’)C₆H₅
In organic chemistry, anilides (or phenylamides) are a class of organic compounds with the general structure R–C(=O)–N(–R’)–C
6H
5. They are amide derivatives of aniline (H
2N–C
6H
5).
Preparation
Aniline reacts with acyl chlorides or carboxylic anhydrides to give anilides. For example, reaction of aniline with acetyl chloride provides acetanilide (CH
3–CO–NH–C
6H
5). At high temperatures, aniline and carboxylic acids react to give anilides.[1]
Uses
- Herbicides[2]
- Fungicides - Oxycarboxin,[3] Carboxin[4]
References
- ↑ Carl N. Webb (1941). "Benzanilide". Organic Syntheses. http://www.orgsyn.org/demo.aspx?prep=cv1p0082.; Collective Volume, 1, pp. 82
- ↑ "Anilide herbicides". Pesticide Target Interaction Database. East China University of Science & Technology. http://lilab.ecust.edu.cn/ptid/compound/browse.html?class=122.
- ↑ PubChem. "Oxycarboxin". National Center for Biotechnology Information. http://pubchem.ncbi.nlm.nih.gov/compound/Oxycarboxin.
- ↑ PubChem. "Carboxin". National Center for Biotechnology Information. http://pubchem.ncbi.nlm.nih.gov/compound/Carboxin.
External links
Original source: https://en.wikipedia.org/wiki/Anilide.
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