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6-Ethyl-5,7-di­methyl-6H-1,4-diazepine-2,3-dicarbo­nitrile

✍ Scribed by Nesterov, Volodymyr V.

Publisher
International Union of Crystallography
Year
2002
Tongue
English
Weight
217 KB
Volume
58
Category
Article
ISSN
1600-5368

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✦ Synopsis

In the title compound, C 11 H 12 N 4 , the diazepine ring exhibits a boat conformation, where the displacements of the C atoms attached to the nitrile groups and the C atom attached to the ethyl group are 0.591 (1), 0.585 (1) and 0.845 (1) A Ê from the base of the boat.

📜 SIMILAR VOLUMES

6-Amino-4-(methyl­sulfanyl)-2-oxo-1-toly
6-Amino-4-(methyl­sulfanyl)-2-oxo-1-tolyl-1,2-di­hydro­pyridine-3,5-dicarbo­nitrile
✍ Elgemeie, Galal H. ;Jones, Peter G. 📂 Article 📅 2004 🏛 International Union of Crystallography 🌐 English ⚖ 244 KB

Single-crystal X-ray study T = 173 K Mean '(C±C) = 0.002 A Ê R factor = 0.033 wR factor = 0.089 Data-to-parameter ratio = 12.7 For details of how these key indicators were automatically derived from the article, see http://journals.iucr.org/e.

2,3-Diphenyl-6,7-dihydro-5H-1,4-diazepin
2,3-Diphenyl-6,7-dihydro-5H-1,4-diazepine
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Zum Thermolyseverhalten von 1,5-Diazabic
Zum Thermolyseverhalten von 1,5-Diazabicyclo[3.3.0]oct-2-enen, 5. Neue einfache Synthesemöglichkeiten für 4,5-Dihydro-1H-1,2-diazepine, 5,6-Dihydro-4H-1,2-diazepine, 4,5,6,7-Tetrahydro-1H-1,2-diazepine und 1-Vinyl-1H-pyrazole
✍ Burger, Klaus ;Schickaneder, Helmut ;Zettl, Claus 📂 Article 📅 1982 🏛 John Wiley and Sons 🌐 English ⚖ 440 KB 👁 1 views

## Abstract 4,4,8,8‐Tetrakis(trifluormethyl)‐1,5‐diazabicyclo[3.3.0]oct‐2‐ene unterliegen bei der Thermolyse, abhängig von den an das bicyclische Skelett gebundenen Substituenten, entweder einer elektrocyclischen Ringöffnung oder einem [3 + 2]‐Cycloreversionsprozeß, dem sich spontan Folgereaktionen