Unknown

Dataset Information

0

(E)-1-(4-Amino-phen-yl)-3-(2,4,5-trimeth-oxy-phen-yl)prop-2-en-1-one.


ABSTRACT: Mol-ecules of the title amino-chalcone, C(18)H(19)NO(4), are twisted, with a dihedral angle of 11.26?(6)° between the 4-amino-phenyl and 2,4,5-trimeth-oxy-phenyl rings. The conformations of the three meth-oxy groups with respect to the benzene ring are slightly different. Two meth-oxy groups are almost coplanar with the attached benzene ring [C-O-C-C torsion angles of -1.45?(19) and 1.5?(2)°], while the third is (-)-synclinal with the attached benzene ring [C-O-C-C = -81.36?(17)°]. In the crystal structure, mol-ecules are stacked into columns along the b axis and mol-ecules in adjacent columns are linked by N-H?O hydrogen bonds into V-shaped double columns. Weak ?-? inter-actions are also observed, with a centroid-centroid distance of 3.7532?(8)?Å.

SUBMITTER: Fun HK 

PROVIDER: S-EPMC3007376 | biostudies-literature | 2010 Jul

REPOSITORIES: biostudies-literature

altmetric image

Publications

(E)-1-(4-Amino-phen-yl)-3-(2,4,5-trimeth-oxy-phen-yl)prop-2-en-1-one.

Fun Hoong-Kun HK   Kobkeatthawin Thawanrat T   Ruanwas Pumsak P   Chantrapromma Suchada S  

Acta crystallographica. Section E, Structure reports online 20100710 Pt 8


Mol-ecules of the title amino-chalcone, C(18)H(19)NO(4), are twisted, with a dihedral angle of 11.26 (6)° between the 4-amino-phenyl and 2,4,5-trimeth-oxy-phenyl rings. The conformations of the three meth-oxy groups with respect to the benzene ring are slightly different. Two meth-oxy groups are almost coplanar with the attached benzene ring [C-O-C-C torsion angles of -1.45 (19) and 1.5 (2)°], while the third is (-)-synclinal with the attached benzene ring [C-O-C-C = -81.36 (17)°]. In the crysta  ...[more]

Similar Datasets

| S-EPMC3200911 | biostudies-literature
| S-EPMC3213527 | biostudies-literature
| S-EPMC3007317 | biostudies-literature
| S-EPMC3200924 | biostudies-literature
| S-EPMC3629594 | biostudies-literature
| S-EPMC3275007 | biostudies-other
| S-EPMC3254497 | biostudies-literature
| S-EPMC3213567 | biostudies-literature
| S-EPMC3120626 | biostudies-literature
| S-EPMC3007858 | biostudies-literature