Dimethoxy-2,3-dimethylbenzene was brominated under radical conditions to give the title compound, C 10 H 11 Br 3 O 4 . The bond lengths and angles are generally within the normal ranges. The crystal packing is stabilized by weak intermolecular C-HÁ Á ÁO and C-HÁ Á ÁBr hydrogen bonds.
1-[3,5-Bis(bromomethyl)-2,4,6-trimethoxybenzyl]-3,5-bis(bromomethyl)-2,4,6-trimethoxybenzene
✍ Scribed by Morgans, G. L. ;Otterlo, W. A. L. van ;Michael, J. P. ;Fernandes, M. A.
- Publisher
- International Union of Crystallography
- Year
- 2005
- Tongue
- English
- Weight
- 389 KB
- Volume
- 62
- Category
- Article
- ISSN
- 1600-5368
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✦ Synopsis
The crystal structure of the title compound, C 23 H 28 Br 4 O 6 , confirms that it consists of two hexasubstituted aromatic units linked by a central methylene group. The molecule lies on a crystallographic twofold axis that passes through the methylene bridging atom. Examination of the extended structure reveals the presence of ribbons of molecules held together by C-HÁ Á ÁO and C-HÁ Á ÁBr interactions.
📜 SIMILAR VOLUMES
In the title compound, C 10 H 12 Br 2 O 2 , all bond lengths and angles are generally within the normal ranges. The crystal packing is stabilized mainly by van der Waals forces.
The title compound, C 23 H 26 BrN 5 O 2 , was synthesized by the reaction of 4- [(2,6-dimethylphenyl)aminocarbonylmethyl]piperazine and 3-(3-nitrophenyl)-5-chloromethyl-1,2,4-oxadiazole. There are intramolecular C-HÁ Á ÁN and intermolecular N-HÁ Á ÁO and C-HÁ Á ÁO hydrogen bonds in the crystal struc