Cathodic behavior of 4,5-dimethoxy-2-nitroamphetamine
✍ Scribed by J. A. Squella; M. Pezzani; Bruce K. Cassels; Milton Aillon-Torres; Marcos C. Rezende; L. J. Nuñez-Vergara
- Book ID
- 102183273
- Publisher
- John Wiley and Sons
- Year
- 1992
- Tongue
- English
- Weight
- 482 KB
- Volume
- 4
- Category
- Article
- ISSN
- 1040-0397
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✦ Synopsis
The amphetamine derivative 4,5-dimethoxy-2-nitrophenyl-2-aminopropane, a positional isomer of the potent hallucinogen DON, was studied by cyclic voltanmetry and polarography. The nitro compound was reduced to the corresponding hydroxylamine under the experimental conditions used.
📜 SIMILAR VOLUMES
The molecule of the title compound, C 16 H 16 N 2 O 5 , a biologically active benzamide derivative, is not planar. The crystal packing is stabilized by C-HÁ Á ÁO and N-HÁ Á ÁO hydrogenbond interactions to form one-dimensional chains parallel to the a axis.
In the asymmetric unit of the title structure, C 13 H 14 N 2 O 2 S, there are two independent molecules. All bond lengths and angles show normal values. The dihedral angles between the phenyl and pyrimidine rings in each molecule are 58.66 (9) and 57.88 ( 8) , but these rings are rotated in opposite
The structure of the title compound, C~23~H~27~N~2~O~4~ ^+^·C~8~H~3~Cl~2~O~4~ ^−^, a 1:1 proton-transfer compound of brucine with 4,5-dichlorophthalic acid, has been determined at 130 K. The brucinium cations and the hydrogen phthalate anions associate through single N—H...O~carboxylate~ hydrogen bo