Karbromal
Karbromal je hipnotik/sedativ. On je originalno sintetisan 1909.[4]
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| Nazivi | |
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| IUPAC naziv
2-Bromo-N-karbamoil-2-etilbutanamid
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| Identifikacija | |
3D model (Jmol)
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| ChemSpider | |
| ECHA InfoCard | 100.000.952 |
| EC broj | 201-046-6 |
| KEGG[1] | |
| MeSH | carbromal |
| UNII | |
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| Svojstva | |
| C7H13BrN2O2 | |
| Molarna masa | 237,10 g·mol−1 |
| Miris | Bez mirisa |
| log P | 1,623 |
| Kiselost (pKa) | 10,69 |
| Baznost (pKb) | 3,31 |
| Srodna jedinjenja | |
Srodne ureje
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Bromizoval |
Srodna jedinjenja
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Ukoliko nije drugačije napomenuto, podaci se odnose na standardno stanje materijala (na 25 °C [77 °F], 100 kPa). | |
| Reference infokutije | |
Vidi još
уредиReference
уреди- ^ Joanne Wixon; Douglas Kell (2000). „Website Review: The Kyoto Encyclopedia of Genes and Genomes — KEGG”. Yeast. 17 (1): 48—55. doi:10.1002/(SICI)1097-0061(200004)17:1<48::AID-YEA2>3.0.CO;2-H.
- ^ 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. PMID 20970519. doi:10.1016/j.drudis.2010.10.003.
- ^ 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.
- ^ DE 225710
