Boyd, PeterLena, GSpicer, Julie2011-09-062008-05ACTA CRYSTALLOGR E 64:O883-U2294 May 20081600-5368https://hdl.handle.net/2292/7734The title compound, C10H13NO3, was obtained as a by-product of the aldolization reaction of furo[3,4-c]pyridin-3(1H)-one with thiophene-2-carboxaldehyde. The substituents on the pyridine ring are nearly coplanar, with an 8.1 (2)degrees rotation of the hydroxmethyl group from this plane. The molecules assemble in the crystal structure as chains via O-H center dot center dot center dot N hydrogen bonding between the pyridine N atom and a neighbouring hydroxymethyl OH group.Items in ResearchSpace are protected by copyright, with all rights reserved, unless otherwise indicated. Previously published items are made available in accordance with the copyright policy of the publisher. Details obtained from http://www.sherpa.ac.uk/romeo/issn/1600-5368/https://researchspace.auckland.ac.nz/docs/uoa-docs/rights.htmhttp://journals.iucr.org/services/copyrightpolicy.htmlEthyl 4-hydroxymethyl-2-methylpyridine-5-carboxylateJournal Article10.1107/S160053680801026XCopyright: International Union of Crystallography21202367http://purl.org/eprint/accessRights/OpenAccess