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Dicikloheksilureja
| Dicikloheksilureja
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| IUPAC ime
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| Identifikacija
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| PubChem[1][2]
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4277
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| ChemSpider[3]
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4126  Y
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| ChEMBL[4]
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CHEMBL1458 Y
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| Jmol-3D slike
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Slika 1
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InChI=1S/C13H24N2O/c16-13(14-11-7-3-1-4-8-11)15-12-9-5-2-6-10-12/h11-12H,1-10H2,(H2,14,15,16) Y
Kod: ADFXKUOMJKEIND-UHFFFAOYSA-N Y
InChI=1/C13H24N2O/c16-13(14-11-7-3-1-4-8-11)15-12-9-5-2-6-10-12/h11-12H,1-10H2,(H2,14,15,16)
Kod: ADFXKUOMJKEIND-UHFFFAOYAR
InChI=1S/C13H24N2O/c16-13(14-11-7-3-1-4-8-11)15-12-9-5-2-6-10-12/h11-12H,1-10H2,(H2,14,15,16)
Kod: ADFXKUOMJKEIND-UHFFFAOYSA-N |
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| Svojstva
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| Molekulska formula
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C13H24N2O
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| Molarna masa
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224.34 g mol−1
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| Opasnost
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| Podaci o bezbednosti prilikom rukovanja (MSDS)
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External MSDS
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| S-oznake
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S24/25
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 Y (šta je ovo?)
(verifikuj)
Ukoliko nije drugačije napomenuto, podaci se odnose na standardno stanje (25 °C, 100 kPa) materijala
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| Infobox references
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Dicikloheksilureja je organsko jedinjenje, iz klase ureja. Ovo jedinjenje je nusproizvod reakcije dicikloheksilkarbodiimida sa aminima ili alkoholima. Ono se može pripremiti reakcijom cikloheksilamina i S,S-dimetil ditiokarbonata.[5]
Reference
- ↑ Li Q, Cheng T, Wang Y, Bryant SH (2010). „PubChem as a public resource for drug discovery.”. Drug Discov Today 15 (23-24): 1052-7. DOI:10.1016/j.drudis.2010.10.003. PMID 20970519. edit
- ↑ Evan E. Bolton, Yanli Wang, Paul A. Thiessen, Stephen H. Bryant (2008). „Chapter 12 PubChem: Integrated Platform of Small Molecules and Biological Activities”. Annual Reports in Computational Chemistry 4: 217-241. DOI:10.1016/S1574-1400(08)00012-1.
- ↑ Hettne KM, Williams AJ, van Mulligen EM, Kleinjans J, Tkachenko V, Kors JA. (2010). „Automatic vs. manual curation of a multi-source chemical dictionary: the impact on text mining”. J Cheminform 2 (1): 3. DOI:10.1186/1758-2946-2-3. PMID 20331846. edit
- ↑ Gaulton A, Bellis LJ, Bento AP, Chambers J, Davies M, Hersey A, Light Y, McGlinchey S, Michalovich D, Al-Lazikani B, Overington JP. (2012). „ChEMBL: a large-scale bioactivity database for drug discovery”. Nucleic Acids Res 40 (Database issue): D1100-7. DOI:10.1093/nar/gkr777. PMID 21948594. edit
- ↑ Man-kit Leung, Jun-Liang Lai, King-Hang Lau, Hsiao-hua Yu, and Hsiang-Ju Hsiao (1996). „S,S-Dimethyl Dithiocarbonate: A Convenient Reagent for the Synthesis of Symmetrical and Unsymmetrical Ureas”. The Journal of Organic Chemistry 61 (12): 4175–4179. DOI:10.1021/jo9522825. PMID 11667305.
Vanjske veze
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