Kogan, Timothy P. et al. published their research in Tetrahedron Letters in 1992 | CAS: 6834-42-0

2-(3-Methoxyphenyl)acetyl chloride (cas: 6834-42-0) belongs to organic chlorides. Organic chlorides are compounds containing a carbon-chlorine bond, which are widely used in the oil field as a wax dissolver. Aliphatic organochlorides are often alkylating agents as chlorine can act as a leaving group, which can result in cellular damage.Application In Synthesis of 2-(3-Methoxyphenyl)acetyl chloride

The synthesis of chiral 3-oxo-6-[(phenylmethoxy)carbonyl]-2-piperazineacetic acid esters designed for the presentation of an aspartic acid side chain. A subsequent novel Friedel Crafts reaction was written by Kogan, Timothy P.;Rawson, Thomas E.. And the article was included in Tetrahedron Letters in 1992.Application In Synthesis of 2-(3-Methoxyphenyl)acetyl chloride This article mentions the following:

The synthesis of the title esters (2S,6R)-I and (2S,6S)-I from L– or D-serine and dimethyl D-malate are described. Acylation of (2S,6S)-I with 3-methoxyphenylacetyl chloride, hydrogenolysis of the benzyl ester, followed by treatment with (COCl)2 then AlCl3 led to unexpected tricyclic product II into which a C2O2 unit had been incorporated. In the experiment, the researchers used many compounds, for example, 2-(3-Methoxyphenyl)acetyl chloride (cas: 6834-42-0Application In Synthesis of 2-(3-Methoxyphenyl)acetyl chloride).

2-(3-Methoxyphenyl)acetyl chloride (cas: 6834-42-0) belongs to organic chlorides. Organic chlorides are compounds containing a carbon-chlorine bond, which are widely used in the oil field as a wax dissolver. Aliphatic organochlorides are often alkylating agents as chlorine can act as a leaving group, which can result in cellular damage.Application In Synthesis of 2-(3-Methoxyphenyl)acetyl chloride

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics