In the title compound, C 17 H 18 O 4 , the hydroxyl and methoxyphenyl substituents are in axial positions. The heterocyclic ring adopts a half-chair conformation. The molecules are linked by OÐHÁ Á ÁO hydrogen bonds, leading to dimerization.
Methyl [5-methoxy-4-(3-methoxyphenyl)isochroman-3-yl]acetate
✍ Scribed by Palusiak, Marcin ;Małecka, Magdalena ;Grabowski, Sławomir J. ;Epsztajn, Jan ;Bieniek, Adam ;Kowalska, Justyna A.
- Publisher
- International Union of Crystallography
- Year
- 2002
- Tongue
- English
- Weight
- 218 KB
- Volume
- 58
- Category
- Article
- ISSN
- 1600-5368
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✦ Synopsis
Single-crystal X-ray study T = 295 K Mean '(C±C) = 0.004 A Ê R factor = 0.055 wR factor = 0.157 Data-to-parameter ratio = 13.7
For details of how these key indicators were automatically derived from the article, see http://journals.iucr.org/e.
📜 SIMILAR VOLUMES
Single-crystal X-ray study T = 293 K Mean '(C±C) = 0.005 A Ê R factor = 0.056 wR factor = 0.186 Data-to-parameter ratio = 14.4 For details of how these key indicators were automatically derived from the article, see http://journals.iucr.org/e.
In the title compound, C 18 H 20 O 5 , the hydroxyl and dimethoxyphenyl substituents are in axial positions. The heterocyclic ring is in a half-chair conformation. The molecules are linked by OÐHÁ Á ÁO hydrogen bonds, leading to the formation of a chain extended throughout the whole of the crystal.
The title compound, C 19 H 18 N 2 O 4 S, was synthesized by the reaction of methyl (2-hydroxyphenyl)acetate and 3-(4-methylthio)phenyl-5-chloromethyl-1,2,4-oxadiazole. The structure exhibits intermolecular CÐHÁ Á ÁO hydrogen bonds and CÐ HÁ Á Á% interactions.