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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.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.otherPURE: 269854019
dc.identifier.otherPURE UUID: ca8a1955-8855-4b17-80fb-93c791d22d73
dc.identifier.otherORCID: /0000-0002-9527-6418/work/79917834
dc.identifier.otherORCID: /0000-0001-6959-5311/work/79917874
dc.identifier.otherScopus: 85090641527
dc.identifier.otherWOS: 000578261800001
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.language.isoeng
dc.relation.ispartofMolbanken
dc.rightsCopyright © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).en
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.description.versionPublisher PDFen
dc.contributor.institutionUniversity of St Andrews. EaSTCHEMen
dc.contributor.institutionUniversity of St Andrews. School of Chemistryen
dc.identifier.doihttps://doi.org/10.3390/M1156
dc.description.statusPeer revieweden
dc.identifier.urlhttps://www.mdpi.com/1422-8599/2020/3/M1156en


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