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  5. Crystal structure and Hirshfeld surface analysis of ethyl 5-phenylisoxazole-3-carboxylate
 
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Crystal structure and Hirshfeld surface analysis of ethyl 5-phenylisoxazole-3-carboxylate

Source
Acta Crystallographica Section E Crystallographic Communications
Date Issued
2017-01-01
Author(s)
Shaik, Althaf
Kirubakaran, Sivapriya  
Thiruvenkatam, Vijay  
DOI
10.1107/S2056989017003127
Volume
73
Abstract
The title compound, C<inf>12</inf>H<inf>11</inf>NO<inf>3</inf>, is an intermediate used in the synthesis of many drug-like molecules. The molecule is almost planar, with the phenyl ring inclined to the isoxazole ring by 0.5(1)°. The ester moiety has an extended conformation and is almost in the same plane with respect to the isoxazole ring, as indicated by the O - C - C - N torsion angle of -172.86(18)°. In the crystal, molecules are linked via pairs of C-H⋯O hydrogen bonds with the same acceptor atom, forming inversion dimers with two R 2<sup>1</sup>(7) ring motifs. The molecules stack in layers lying parallel to (10-3). Analysis using Hirshfeld surface generation and two-dimensional fingerprint plots explores the distribution of weak intermolecular interactions in the crystal structure.
Publication link
http://journals.iucr.org/e/issues/2017/04/00/su5350/su5350.pdf
URI
http://repository.iitgn.ac.in/handle/IITG2025/22570
Subjects
crystal structure | drug intermediate | Hirshfeld surface | hydrogen bonding | isoxazole derivative
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