(5-Chloro-1,3-benzoxazol-2-ylthio)acetonitrile
| dc.contributor.author | Ergin, Ömer | |
| dc.contributor.author | Sıllanpaa, Reijo | |
| dc.contributor.author | Şafak, Cihat | |
| dc.contributor.author | Çalış, İhsan | |
| dc.date.accessioned | 2019-10-17T06:40:06Z | |
| dc.date.available | 2019-10-17T06:40:06Z | |
| dc.date.issued | 1994 | en_US |
| dc.department | Fakülteler, Necatibey Eğitim Fakültesi, Matematik ve Fen Bilimleri Eğitimi Bölümü | en_US |
| dc.description | Ergin Ömer (Balikesir Author) | en_US |
| dc.description.abstract | 5-Chloro-1,3-benzoxazol-2-ylthio)acetonitrile, C9H5-ClN2OS, was obtained by the reaction of chloro acetonitrile with 5-chloro-2-mercaptobenzoxazole. The structure of the title compound was indicated by IR, H-1 NMR and C-13 NMR spectra, and confirmed by an X-ray analysis. The cyanomethyl group is bonded to the benzoxazole ring through the S atom. The starting compound reacts in the thiol form. Intermolecular bonding includes C-H...N hydrogen bonds. | en_US |
| dc.identifier.doi | 10.1016/0969-8043(95)00229-4 | |
| dc.identifier.endpage | 935 | en_US |
| dc.identifier.issn | 0108-2701 | |
| dc.identifier.issue | Part 6 | en_US |
| dc.identifier.startpage | 933 | en_US |
| dc.identifier.uri | http.//10.1016/0969-8043(95) 00229-4 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.12462/7341 | |
| dc.identifier.volume | 50 | en_US |
| dc.identifier.wos | WOS:A1994NT50900042 | |
| dc.identifier.wosquality | N/A | |
| dc.indekslendigikaynak | Web of Science | |
| dc.language.iso | en | en_US |
| dc.publisher | Munksgaard Int Publ Ltd | en_US |
| dc.relation.ispartof | Acta Crystallographıca Sectıon C-Crystal Structure Communıcatıonsi | en_US |
| dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
| dc.rights | info:eu-repo/semantics/closedAccess | en_US |
| dc.title | (5-Chloro-1,3-benzoxazol-2-ylthio)acetonitrile | en_US |
| dc.type | Article | en_US |
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