Unknown

Dataset Information

0

Crystal structure of (E)-2-hy-droxy-4'-meth-oxy-aza-stilbene.


ABSTRACT: The title aza-stilbene derivative, C14H13NO2 {systematic name: (E)-2-[(4-meth-oxy-benzyl-idene)amino]-phenol}, is a product of the condensation reaction between 4-meth-oxy-benzaldehyde and 2-amino-phenol. The mol-ecule adopts an E conformation with respect to the azomethine C=N bond and is almost planar, the dihedral angle between the two substituted benzene rings being 3.29 (4)°. The meth-oxy group is coplanar with the benzene ring to which it is attached, the Cmeth-yl-O-C-C torsion angle being -1.14 (12)°. There is an intra-molecular O-H⋯N hydrogen bond generating an S(5) ring motif. In the crystal, mol-ecules are linked via C-H⋯O hydrogen bonds, forming zigzag chains along [10-1]. The chains are linked via C-H⋯π inter-actions, forming a three-dimensional structure.

SUBMITTER: Chantrapromma S 

PROVIDER: S-EPMC4459367 | biostudies-literature | 2015 Jun

REPOSITORIES: biostudies-literature

altmetric image

Publications

Crystal structure of (E)-2-hy-droxy-4'-meth-oxy-aza-stilbene.

Chantrapromma Suchada S   Kaewmanee Narissara N   Boonnak Nawong N   Chantrapromma Kan K   Ghabbour Hazem A HA   Fun Hoong-Kun HK  

Acta crystallographica. Section E, Crystallographic communications 20150507 Pt 6


The title aza-stilbene derivative, C14H13NO2 {systematic name: (E)-2-[(4-meth-oxy-benzyl-idene)amino]-phenol}, is a product of the condensation reaction between 4-meth-oxy-benzaldehyde and 2-amino-phenol. The mol-ecule adopts an E conformation with respect to the azomethine C=N bond and is almost planar, the dihedral angle between the two substituted benzene rings being 3.29 (4)°. The meth-oxy group is coplanar with the benzene ring to which it is attached, the Cmeth-yl-O-C-C torsion angle being  ...[more]

Similar Datasets

| S-EPMC4571386 | biostudies-literature
| S-EPMC4645031 | biostudies-literature
| S-EPMC6002819 | biostudies-literature
| S-EPMC4992913 | biostudies-literature
| S-EPMC4518918 | biostudies-literature
| S-EPMC3006953 | biostudies-literature
| S-EPMC2983260 | biostudies-literature
| S-EPMC6362667 | biostudies-literature
| S-EPMC4992917 | biostudies-literature
| S-EPMC3588809 | biostudies-other