The title compound, C 13 H 14 O 3 S, was prepared by alkaline hydrolysis of ethyl 2-(5-ethyl-3-methylsulfanyl-1-benzofuran-2-yl)acetate. The crystal structure is stabilized by aromaticstacking interactions and inversion-related intermolecular O-HÁ Á ÁO hydrogen bonds between adjacent carboxyl groups
✦ LIBER ✦
The Metabolic Fate of 5-(bicyclo-3, 2, 1-oct-2-en-2-yl)-5-ethyl Barbituric Acid, (Reposal ®).
✍ Scribed by Nielsen, P. ;Tarding, F.
- Book ID
- 114798582
- Publisher
- Wiley (Blackwell Publishing)
- Year
- 2009
- Weight
- 440 KB
- Volume
- 26
- Category
- Article
- ISSN
- 0001-6683
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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
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