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2,4,6-Trimethylbenzyl chloride (α2-chloroisodurene)

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dc.contributor.authorAitken, R Alan
dc.contributor.authorSlawin, Alexandra Martha Zoya
dc.date.accessioned2020-09-01T16:30:01Z
dc.date.available2020-09-01T16:30:01Z
dc.date.issued2020-09-01
dc.identifier269854019
dc.identifierca8a1955-8855-4b17-80fb-93c791d22d73
dc.identifier85090641527
dc.identifier000578261800001
dc.identifier.citationAitken , R A & Slawin , A M Z 2020 , ' 2,4,6-Trimethylbenzyl chloride (α 2 -chloroisodurene) ' , Molbank , vol. 2020 , no. 3 , M1156 . https://doi.org/10.3390/M1156en
dc.identifier.issn1422-8599
dc.identifier.otherORCID: /0000-0002-9527-6418/work/79917834
dc.identifier.otherORCID: /0000-0001-6959-5311/work/79917874
dc.identifier.urihttps://hdl.handle.net/10023/20533
dc.description.abstractThe X-ray structure of the title compound has been determined and it is compared with those of other substituted benzyl chlorides reported previously. It has an atypically long CH2–Cl bond.
dc.format.extent4
dc.format.extent764720
dc.language.isoeng
dc.relation.ispartofMolbanken
dc.subject2,4,6-trimethylbenzyl chlorideen
dc.subjectX-ray structureen
dc.subjectC–Cl bond lengthen
dc.subjectQD Chemistryen
dc.subjectDASen
dc.subject.lccQDen
dc.title2,4,6-Trimethylbenzyl chloride (α2-chloroisodurene)en
dc.typeJournal articleen
dc.contributor.institutionUniversity of St Andrews. EaSTCHEMen
dc.contributor.institutionUniversity of St Andrews. School of Chemistryen
dc.identifier.doi10.3390/M1156
dc.description.statusPeer revieweden
dc.identifier.urlhttps://www.mdpi.com/1422-8599/2020/3/M1156en


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