The asymmetric unit of the title compound, C 10 H 26 N 2 O 2 2+ Á-2NO 3 À , comprises one half of an N-diprotonated (R,S)ethambutol cation, which lies about a centre of symmetry, and a nitrate anion. In the crystal structure, a two-dimensional network is formed via intermolecular O-HÁ Á ÁO and N-HÁ
(2R,2′S)-2,2′-(Ethane-1,2-diyldiiminio)bis(butane-2,1-diyl) disulfate dihydrate
✍ Scribed by Bai, Guo-Yi ;Zhang, Chen-Fang ;Simpson, Jim ;Chen, Yong ;Peng, Hong-Wei
- Publisher
- International Union of Crystallography
- Year
- 2007
- Tongue
- English
- Weight
- 233 KB
- Volume
- 63
- Category
- Article
- ISSN
- 1600-5368
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✦ Synopsis
The title compound, C~10~H~28~N~2~O~10~S~2~, was synthesized by the reaction of concentrated sulfuric acid with (R,S)-ethambutol. The zwitterionic amino–sulfate system, protonated at both N atoms, lies about a centre of symmetry. The asymmetric unit also contains a solvent water molecule. In the crystal structure, intermolecular O—H...N and N—H...O hydrogen bonds link the molecules into a three-dimensional network.
📜 SIMILAR VOLUMES
In the title compound, [Fe 2 (C 5 H 5 ) 2 (C 26 H 20 N 4 )], two ferrocene units are bridged by a Schiff base linker with an intramolecular FeÁ Á ÁFe separation of 7.42 (2) A ˚.
The title compound, C~20~H~24~N~4~ ^2+^·2Br^−^·2H~2~O, was prepared from benzimidazole by stepwise alkylation with ethyl bromide followed by 1,2-bromoethane. The dication lies about a twofold rotation axis through the centre of the ethanyl group that links the two planar benzimidazolium residues. Th