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.
2-Amino-4-(2-naphthyl)thiophene-3-carbonitrile
✍ Scribed by Çoruh, Ufuk ;Tümer, Ferhan ;Vázquez-López, Ezequiel M. ;Demir, Ümit
- Publisher
- International Union of Crystallography
- Year
- 2005
- Tongue
- English
- Weight
- 375 KB
- Volume
- 61
- Category
- Article
- ISSN
- 1600-5368
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✦ Synopsis
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 thiophene, which are nearly perpendicular to one another. In the crystal structure, a hydrogen bond, with a DÁ Á ÁA distance of 3.033 (3) A ˚, is present between the amino substituent and the carbonitrile N atom of a symmetry-related molecule. The crystal structure also includes one C-HÁ Á Á interaction.
📜 SIMILAR VOLUMES
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.
In the crystal structure of the title compound, C~6~H~6~I~2~S, the molecules pack to form one-dimensional chains connected by intermolecular S...I interactions.
In the title compound, [Fe(C 5 H 5 )(C 17 H 10 Cl 2 N 3 )], the planes of the substituted cyclopentadienyl and benzene rings make dihedral angles of 14.3 (2) and 87.2 (1) , respectively, with the pyridine ring.