Abstract
In the racemic title compound, C20H16N2O5, the pyran ring adopts a shallow envelope conformation, with the stereogenic C atom displaced from the other atoms by 0.273 (2) Å. The dihedral angle between the fused-ring system and the pendant p-tolyl group is 87.62 (7)°. The molecular conformation is consolidated by an intramolecular N - H⋯O hydrogen bond, which generates an S(6) ring. In the crystal, molecules are linked by C - H⋯O interactions, resulting in [010] chains.
Original language | English |
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Pages (from-to) | o158-o159 |
Number of pages | 2 |
Journal | Acta Crystallographica Section E: Structure Reports Online |
Volume | 71 |
Issue number | 3 |
Early online date | 7 Feb 2015 |
DOIs | |
Publication status | Published - 1 Mar 2015 |
Bibliographical note
The authors thank Dr Babu Varghese, SAIF, IIT, Chennai, India, for the data collection.Keywords
- Biological activity
- Chromene derivatives
- Crystal structure
- Hydrogen bonding
- Pyrano[3,2-c]chromenone