Unknown

Dataset Information

0

(2E)-1-(Pyridin-2-yl)-3-(2,4,6-trimeth-oxy-phen-yl)prop-2-en-1-one.


ABSTRACT: The title heteroaryl chalcone derivative, C(17)H(17)NO(4), is a condensation product of 2-acetyl-pyridine and 2,4,6-trimeth-oxy-benzaldehyde. The mol-ecule is roughly planar, the dihedral angle between the pyridine and benzene rings being 5.51?(10)°. All the three meth-oxy groups are almost co-planar with the bound benzene ring [r.m.s. deviation of 0.0306?(2)?Å]. A weak C-H?O intra-molecular inter-action involving one of the ortho-meth-oxy groups generates an S(6) ring motif. In the crystal, the mol-ecules are linked by weak C-H?O inter-actions into anti-parallel face-to-face pairs. Adjacent pairs are further connected into sheets parallel to the ab plane.

SUBMITTER: Fun HK 

PROVIDER: S-EPMC3201482 | biostudies-literature | 2011 Oct

REPOSITORIES: biostudies-literature

altmetric image

Publications

(2E)-1-(Pyridin-2-yl)-3-(2,4,6-trimeth-oxy-phen-yl)prop-2-en-1-one.

Fun Hoong-Kun HK   Chantrapromma Suchada S   Suwunwong Thitipone T  

Acta crystallographica. Section E, Structure reports online 20110930 Pt 10


The title heteroaryl chalcone derivative, C(17)H(17)NO(4), is a condensation product of 2-acetyl-pyridine and 2,4,6-trimeth-oxy-benzaldehyde. The mol-ecule is roughly planar, the dihedral angle between the pyridine and benzene rings being 5.51 (10)°. All the three meth-oxy groups are almost co-planar with the bound benzene ring [r.m.s. deviation of 0.0306 (2) Å]. A weak C-H⋯O intra-molecular inter-action involving one of the ortho-meth-oxy groups generates an S(6) ring motif. In the crystal, the  ...[more]

Similar Datasets

| S-EPMC3515281 | biostudies-literature
| S-EPMC3120626 | biostudies-literature
| S-EPMC3006788 | biostudies-literature
| S-EPMC3344577 | biostudies-literature
| S-EPMC2983191 | biostudies-literature
| S-EPMC3200663 | biostudies-literature
| S-EPMC3213527 | biostudies-literature
| S-EPMC3254417 | biostudies-literature
| S-EPMC3770358 | biostudies-literature
| S-EPMC2983143 | biostudies-literature