Year-end Sale % OFF 
Abstract
In the title compound, C17H13NO2, the benzene ring is twisted slightly out of the plane of the oxazole ring to which it is attached [dihedral angle = 7.98 (8)°]. Similarly, there is a twist [dihedral angle = 5.50 (8)°] between the oxazole and phenyl rings that are linked via the C=C bond [1.348 (2) Å]; the conformation about the latter is Z. In the crystal, the presence of C—H⋯O, C—H⋯π and π–π interactions [centroid–centroid distance = 3.5259 (9) Å] link the molecules into a three-dimensional architecture.
Highlights
In the paper by Asiri et al [Acta Cryst. (2012), E68, o1154], the title and the chemical name of one of the reagents used in the synthesis are corrected
In the paper by Asiri et al (2012), the chemical name given in the title should be ‘(4Z)-4-Benzylidene-2-(4-methylphenyl)1,3-oxazol-5(4H)-one’
[dihedral angle = 5.50 (8) ] between the oxazole and phenyl rings that are linked via the C C bond [1.348 (2) Å]; the conformation about the latter is Z
Summary
R factor = 0.044; wR factor = 0.109; data-to-parameter ratio = 16.4. C17H13NO2, the benzene ring is twisted slightly out of the plane of the oxazole ring to which it is attached [dihedral angle = 7.98 (8) ]. There is a twist [dihedral angle = 5.50 (8) ] between the oxazole and phenyl rings that are linked via the C C bond [1.348 (2) Å]; the conformation about the latter is Z. The presence of C—H O, C—H and – interactions [centroid–. Centroid distance = 3.5259 (9) Å] link the molecules into a three-dimensional architecture. Cg1 is the centroid of the C5–C10 ring. Symmetry codes: (i) x 12; y; z þ 32; (ii) x þ 32; y þ 12; z þ 1; (iii) x; y 32; z 12. Data collection: CrysAlis PRO (Agilent, 2011); cell refinement: CrysAlis PRO; data reduction: CrysAlis PRO; program(s) used to solve structure: SHELXS97 (Sheldrick, 2008); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008); molecular graphics: ORTEP-3 (Farrugia, 1997) and DIAMOND (Brandenburg, 2006); software used to prepare material for publication: publCIF (Westrip, 2010)
Sign-in/Register to view highlights & summary 
Published Version (
Free)
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callMore From: Acta Crystallographica Section E Structure Reports Online
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
