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2-Amino-4-methyl­thio­phene-3-carbo­nitrile

✍ Scribed by Çoruh, Ufuk ;Ustabaş, Reşat ;Tümer, Ferhan ;García-Granda, Santiago ;Demir, Ümit ;Ekinci, Duygu ;Yavuz, Metin


Publisher
International Union of Crystallography
Year
2003
Tongue
English
Weight
204 KB
Volume
59
Category
Article
ISSN
1600-5368

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✦ Synopsis


The title compound, C 6 H 6 N 2 S, consists of a thiophene ring carrying three substitutent groups. Two NÐHÁ Á ÁN intermolecular hydrogen bonds link neighboring molecules into a threedimensional network.


📜 SIMILAR VOLUMES


2-Amino-4-(2-naphthyl)­thio­phene-3-carb
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A new type of thiophene derivative with potential pharmacological activity, viz. 2-amino-4-(2-naphthalyl)thiophene-3carbonitrile, C 15 H 10 N 2 S, has been prepared and studied by NMR and single-crystal X-ray diffraction techniques. The molecule contains two different groups, naphthalene and thiophe

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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.

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The structure of the title compound, C 7 H 9 NO 2 S, forms a supramolecular network. The planar sheet structure displays both intra-and intermolecular N-HÁ Á ÁO hydrogen bonding. The asymmetric unit consists of two molecules.

4′-Bromo­methyl­bi­phenyl-2-carbo­nitril
✍ Song, Qing-Bao ;Li, Yi-Zhi ;Qi, Chen-Ze ;Shen, Tian-Hua ;Wang, Hai-Bin 📂 Article 📅 2003 🏛 International Union of Crystallography 🌐 English ⚖ 305 KB

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.

6-Amino-4-[4-(di­methyl­amino)­phenyl]-3
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Single-crystal X-ray study T = 193 K Mean '(C±C) = 0.002 A Ê R factor = 0.041 wR factor = 0.103 Data-to-parameter ratio = 12.4 For details of how these key indicators were automatically derived from the article, see http://journals.iucr.org/e.