Please use this identifier to cite or link to this item: https://doi.org/10.1107/S1600536811003679
Title: Nitrofurantoin methanol monosolvate
Authors: Vangala, V.R.
Chow, P.S.
Tan, R.B.H. 
Issue Date: Mar-2011
Source: Vangala, V.R., Chow, P.S., Tan, R.B.H. (2011-03). Nitrofurantoin methanol monosolvate. Acta Crystallographica Section E: Structure Reports Online 67 (3) : o550-o551. ScholarBank@NUS Repository. https://doi.org/10.1107/S1600536811003679
Abstract: The antibiotic nitrofurantoin {systematic name: (E)-1-[(5-nitro-2-furyl) methylideneamino]imidazolidine-2,4-dione} crystallizes as a methanol monosolvate, C8H6N4O5·CH 4O. The nitrofurantoin molecule adopts a nearly planar conformation (r.m.s. deviation = 0.0344 Å). Hydrogen bonds involve the co-operative N - H⋯O - H⋯O heterosynthons between the cyclic imide of nitrofurantoin and methanol O - H groups. There are also C - H⋯O hydrogen bonds involving the nitrofurantoin molecules which support the key hydrogen-bonding synthon. The overall crystal packing is further assisted by weak C - H⋯O interactions, giving a herringbone pattern.
Source Title: Acta Crystallographica Section E: Structure Reports Online
URI: http://scholarbank.nus.edu.sg/handle/10635/89585
ISSN: 16005368
DOI: 10.1107/S1600536811003679
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