1H-Imidazole-4-carbonitrile
✍ Scribed by Less, Gregory B. ;Rasmussen, Paul G. ;Kampf, Jeff W.
- Book ID
- 104484202
- Publisher
- International Union of Crystallography
- Year
- 2005
- Tongue
- English
- Weight
- 181 KB
- Volume
- 61
- Category
- Article
- ISSN
- 1600-5368
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✦ Synopsis
The title compound, C 4 H 3 N 3 , was synthesized in three steps from diaminomaleonitrile in an overall yield of 38%. Singlecrystal X-ray analysis reveals that the compound crystallizes exclusively as the 1H-imidazole-4-carbonitrile isomer. This heterocycle forms a non-centrosymmetric crystal structure and packs with an appreciable dipole moment, making it a good candidate for non-linear optical applications.
📜 SIMILAR VOLUMES
The title compound, C 22 H 21 ClN 4 O, is used as an intermediate for the synthesis of biologically active compounds. Geometric parameters are in the usual ranges. The packing is stabilized by O-HÁ Á ÁN hydrogen bonding.
Single-crystal X-ray study T = 293 K Mean '(C±C) = 0.007 A Ê R factor = 0.045 wR factor = 0.088 Data-to-parameter ratio = 15.8 For details of how these key indicators were automatically derived from the article, see http://journals.iucr.org/e.
Single-crystal X-ray study T = 90 K Mean '(C±C) = 0.004 A Ê R factor = 0.044 wR factor = 0.098 Data-to-parameter ratio = 13.7 For details of how these key indicators were automatically derived from the article, see http://journals.iucr.org/e.