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Ethyl 4-amino-5-cyano-6-[(2-hydroxyethyl)amino]-2-methylnicotinate

✍ Scribed by Ren, Qing-Yun ;He, Hong-Wu ;Jin, Chuan-Fei ;Gu, Yu-Cheng


Publisher
International Union of Crystallography
Year
2007
Tongue
English
Weight
999 KB
Volume
63
Category
Article
ISSN
1600-5368

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✦ Synopsis


In the title compound, C 12 H 16 N 4 O 3 , all bond lengths and angles are within normal ranges. An O-HÁ Á ÁN and an N-HÁ Á ÁO intramolecular hydrogen bond contribute to the approximately planar molecular conformation. In the crystal structure, intermolecular N-HÁ Á ÁO and N-HÁ Á ÁN hydrogen bonds link the molecules into ribbons parallel to the [110] direction.


📜 SIMILAR VOLUMES


Ethyl 4-amino-5-cyano-2-methyl-6-(2-nitr
✍ Ren, Qing-Yun ;He, Hong-Wu ;Yao, Yong-Yan ;Gu, Yu-Cheng 📂 Article 📅 2007 🏛 International Union of Crystallography 🌐 English ⚖ 472 KB

In the title compound, C~16~H~14~N~4~O~5~, the benzene ring of the nicotinate residue is inclined at an angle of 64.06 (10)° to the benzene ring of the nitrophenoxy group. The molecules are linked by two intermolecular C—H...O and N—H...N hydrogen bonds into a complex three-dimensional framework str

Ethyl 6-amino-2-(chloromethyl)-5-cyano-4
✍ Athimoolam, S. ;Devi, N. Savitha ;Bahadur, S. Asath ;Kannan, R. Sayee ;Perumal, 📂 Article 📅 2007 🏛 International Union of Crystallography 🌐 English ⚖ 854 KB

In the title compound, C 17 H 17 ClN 2 O 3 , the six-membered pyran ring adopts a near-boat conformation. The crystal packing features two intramolecular C-HÁ Á ÁO interactions and the crystal structure is stabilized by intermolecular N-HÁ Á ÁO hydrogen bonds. These lead to two primary motifs, viz.

4,5-Di­cyano-1,2-bis(2-di­methyl­amino­e
✍ Çoruh, Ufuk ;Ustabaş, Reşat ;Yılmaz, İsmail ;Yavuz, Metin 📂 Article 📅 2003 🏛 International Union of Crystallography 🌐 English ⚖ 171 KB

Single-crystal X-ray study T = 293 K Mean '(C±C) = 0.004 A Ê R factor = 0.045 wR factor = 0.095 Data-to-parameter ratio = 21.9 For details of how these key indicators were automatically derived from the article, see http://journals.iucr.org/e.