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{{Short description|Group of chemical compounds}}
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[[File:Anisoyl chloride isomers.svg|300px|thumb|[[Arene substitution patterns|Positional isomers]] of anisoyl chloride: ''ortho'' (2-methoxybenzoyl chloride), ''meta'' (3-methoxybenzoyl chloride), and ''para'' (4-methoxybenzoyl chloride)]]
| Name = Anisoyl chloride
| ImageFile = Anisoylchloride.png
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| ImageName = Anisoyl chloride
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|C=8|H=7|Cl=1|O=2
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There are three [[isomers]] of '''anisoyl chloride''' (also called '''methoxybenzoyl chloride''') which are [[chemical compounds]]. There are the ''ortho-'', ''meta-'', and ''para-'' forms. These [[organic compound]]s belong in the class of [[acyl halide]]s, specifically [[aromatic]] acyl chlorides.


'''Anisoyl chloride''' (also called '''methoxybenzoyl chloride''') is an [[acyl halide]], specifically an [[aromatic]] acyl chloride, and may be formed from [[anisic acid]] by replacing a [[hydroxyl]] group of the [[carboxylic acid]] with a [[chloride]] group. There are three [[isomers]]: the ''ortho-'', ''meta-'', and ''para-'' forms. Their structures differ in the [[arene substitution pattern]]—the location of the [[methoxy]] group on the ring as compared to the acyl halide.

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==References==
==References==
* [http://webbook.nist.gov/cgi/cbook.cgi?ID=C100072 National Institute of Standards and Technology (NIST) reference data for anisoyl chloride]
{{Unreferenced|date =September 2007}}
* [https://echa.europa.eu/substance-information/-/substanceinfo/100.002.561]
<references/>

{{aromatic-stub}}
{{aromatic-stub}}
[[Category:Aromatic compounds]]
[[Category:Benzene derivatives]]
[[Category:Acyl chlorides]]
[[Category:Acyl chlorides]]
[[Category:Phenol ethers]]
[[Category:Phenol ethers]]

Latest revision as of 20:59, 2 October 2021

Positional isomers of anisoyl chloride: ortho (2-methoxybenzoyl chloride), meta (3-methoxybenzoyl chloride), and para (4-methoxybenzoyl chloride)

Anisoyl chloride (also called methoxybenzoyl chloride) is an acyl halide, specifically an aromatic acyl chloride, and may be formed from anisic acid by replacing a hydroxyl group of the carboxylic acid with a chloride group. There are three isomers: the ortho-, meta-, and para- forms. Their structures differ in the arene substitution pattern—the location of the methoxy group on the ring as compared to the acyl halide.

References[edit]

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