Wikipedia:WikiProject Chemicals/Chembox validation/VerifiedDataSandbox and Terbuthylazine: Difference between pages
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Saving copy of the {{chembox}} taken from revid 444217414 of page Terbuthylazine for the Chem/Drugbox validation project (updated: ''). |
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{{more citations needed|date=January 2021}} |
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{{ambox | text = This page contains a copy of the infobox ({{tl|chembox}}) taken from revid [{{fullurl:Terbuthylazine|oldid=444217414}} 444217414] of page [[Terbuthylazine]] with values updated to verified values.}} |
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{{chembox |
{{chembox |
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| verifiedrevid = |
| verifiedrevid = 470602280 |
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|ImageFile=Terbuthylazine.png |
| ImageFile = Terbuthylazine.png |
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| ImageAlt = Skeletal formula of terbuthylazine |
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|ImageSize= |
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| ImageFile1 = Terbuthylazine-3D-spacefill.png |
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| ImageAlt1 = Space-filling model of the terbuthylazine molecule |
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|Section1={{Chembox Identifiers |
|Section1={{Chembox Identifiers |
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| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} |
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| ChemSpiderID = 20848 |
| ChemSpiderID = 20848 |
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| InChI = 1/C9H16ClN5/c1-5-11-7-12-6(10)13-8(14-7)15-9(2,3)4/h5H2,1-4H3,(H2,11,12,13,14,15) |
| InChI = 1/C9H16ClN5/c1-5-11-7-12-6(10)13-8(14-7)15-9(2,3)4/h5H2,1-4H3,(H2,11,12,13,14,15) |
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| CASNo_Ref = {{cascite|correct|CAS}} |
| CASNo_Ref = {{cascite|correct|CAS}} |
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| CASNo=5915-41-3 |
| CASNo=5915-41-3 |
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| UNII_Ref = {{fdacite|correct|FDA}} |
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| UNII = M095B391J7 |
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| KEGG_Ref = {{keggcite|correct|kegg}} |
| KEGG_Ref = {{keggcite|correct|kegg}} |
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| KEGG = C18810 |
| KEGG = C18810 |
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| ChEBI_Ref = {{ebicite|correct|EBI}} |
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| ChEBI = 30263 |
| ChEBI = 30263 |
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| SMILES = Clc1nc(nc(n1)NC(C)(C)C)NCC |
| SMILES = Clc1nc(nc(n1)NC(C)(C)C)NCC |
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}} |
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|Section2={{Chembox Properties |
|Section2={{Chembox Properties |
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| Formula=C<sub>9</sub>H<sub>16</sub>ClN<sub>5</sub> |
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| MolarMass=229.710 g/mol |
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|Section3={{Chembox Hazards |
|Section3={{Chembox Hazards |
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| MainHazards= |
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| FlashPt= |
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| AutoignitionPt = |
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| Autoignition= |
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'''Terbuthylazine''' is a selective [[herbicide]]. Chemically, it is a halogenated [[triazine]]; compared with [[atrazine]] and [[simazine]], it has a [[tert-butyl]] group in place of the [[isopropyl]] and [[ethyl group|ethyl]] groups, respectively.<ref>{{cite journal|title=Sorption of terbuthylazine and atrazine in relation to the physico-chemical properties of three soils|journal=[[Chemosphere (journal)|Chemosphere]]|volume=28|issue=3|pages=467–476|doi=10.1016/0045-6535(94)90291-7|year=1994|last1=Dousset|first1=S.|last2=Mouvet|first2=C.|last3=Schiavon|first3=M.|bibcode=1994Chmsp..28..467D }}</ref><ref>{{cite journal|title=Dissipation of terbuthylazine, metolachlor, and mesotrione in soils with contrasting texture|journal=[[J Environ Sci Health B]]|volume=53|issue=10|pages=661–668|doi=10.1080/03601234.2018.1474556|year=2018|last1=Carretta|first1=L.|last2=Cardinali|first2=A.|last3=Marotta|first3=E.|last4=Zanin|first4=G.|last5=Masin|first5=R.|pmid=29842837|bibcode=2018JESHB..53..661C |s2cid=44163175 }}</ref> |
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==Referenced== |
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{{reflist}} |
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{{Herbicides}} |
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[[Category:Herbicides]] |
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[[Category:Triazines]] |
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[[Category:Chloroarenes]] |
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[[Category:Tert-butyl compounds]] |
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