In the title molecule, C 17 H 14 Cl 2 O 3 , the methoxy groups are almost coplanar with the attached benzene ring. The molecules are linked via intermolecular C-HÁ Á ÁO interactions into wave-like chains along the b axis.
O-Ethyl S-[1-(3,4-dimethoxyphenyl)-2-(hydroxyimino)propyl] dithiocarbonate
✍ Scribed by Hartung, Jens ;Daniel, Kristina ;Svoboda, Ingrid ;Fuess, Hartmut
- Book ID
- 104485286
- Publisher
- International Union of Crystallography
- Year
- 2005
- Tongue
- English
- Weight
- 142 KB
- Volume
- 61
- Category
- Article
- ISSN
- 1600-5368
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✦ Synopsis
The stereogenic centre in the title compound, C 14 H 19 NO 4 S 2 , is substituted with a dithiocarbonate, an ethyloximino and a 3,4dimethoxyphenyl group, as well as an H atom. Tandem hydrogen-bonding occurs between enantiomers to produce dimers, in which the oxime H atom serves as donor toward the oxime N atom of an adjacent molecule.
📜 SIMILAR VOLUMES
In the title biologically active compound, C 17 H 13 Cl 2 FO 3 , the central C C double bond is trans configured. The molecule consists of two essentially planar parts which are twisted by 67.06 (2) with respect to each other.
In the title cocrystal, 0.893C 19 H 20 O 4 Á0.104C 18 H 17 ClO 3 Á-0.003C 17 H 14 Cl 2 O, the crystal packing is stabilized by weak intermolecular C-HÁ Á ÁO and C-HÁ Á Á interactions.
In the title compound, C 18 H 16 O 6 , a herbicide, the dioxole ring adopts a flattened envelope conformation. The two aromatic rings at either end of the propenone linkage are almost coplanar with it. The hydroxy group is involved in an intramolecular O-HÁ Á ÁO hydrogen bond.