3-[(2,4,6-Trichloroanilino)carbonyl]prop-2-enoic acid
✍ Scribed by Parvez, Masood ;Shahzadi, Saira ;Shahid, Khadija ;Ali, Saqib
- Book ID
- 104482765
- Publisher
- International Union of Crystallography
- Year
- 2004
- Tongue
- English
- Weight
- 341 KB
- Volume
- 60
- Category
- Article
- ISSN
- 1600-5368
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✦ Synopsis
The crystal structure of the title compound, C 10 H 6 Cl 3 NO 3 , establishes that condensation of 2,4,6-trichloroaniline with maleic anhydride gives the title compound at room temperature. There are strong intermolecular NÐHÁ Á ÁO hydrogen bonds [NÁ Á ÁO = 2.832 (2) and 2.867 (2) A Ê ], resulting in a hydrophobic region in the middle of the unit cell. The carboxyl groups adopt an anti-planar conformation and participate in intramolecular OÐHÁ Á ÁO hydrogen bonds [both OÁ Á ÁO = 2.486 (2) A Ê ]. There are two molecules in the asymmetric unit.
📜 SIMILAR VOLUMES
In the title molecule, C 15 H 9 BrClFO, the dihedral angle between the two benzene rings is 22.7 (1) . The crystal structure is stabilized by intermolecular C-HÁ Á ÁF interactions and short BrÁ Á ÁCl contacts [BrÁ Á ÁCl = 3.579 (1) A ˚]. The compound can potentially exhibit second-order nonlinear op
## Abstract LC/MS^3^‐Guided biotransformation of __p__‐coumaric acid (=(2__E__)‐3‐(4‐hydroxyphenyl)prop‐2‐enoic acid; CA) with H~2~O~2~/__Momordica charantia__ peroxidase at pH 5.0 and 45° in the presence of acetone has resulted in the isolation of three CA trimers, triCA1 (**1**), triCA2 (__trans_
Single-crystal X-ray study T = 298 K Mean '(C±C) = 0.006 A Ê R factor = 0.063 wR factor = 0.185 Data-to-parameter ratio = 15.4 For details of how these key indicators were automatically derived from the article, see http://journals.iucr.org/e.