The bicyclo[3.1.0]hexane fragment of the title molecule, C 9 H 12 O 4 , adopts a boat-like conformation, with its methoxycarbonyl substituent in the endo position. In the crystal structure, molecules form centrosymmetric OÐHÁ Á ÁO hydrogen-bonded dimers, which are arranged in layers.
Succinimido 4-(N-maleimidomethyl)cyclohexanecarboxylate
✍ Scribed by Brown, Christopher L. ;Atkinson, Sarah J. ;Healy, Peter C.
- Publisher
- International Union of Crystallography
- Year
- 2005
- Tongue
- English
- Weight
- 123 KB
- Volume
- 61
- Category
- Article
- ISSN
- 1600-5368
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✦ Synopsis
The title compound {alternative name: 2,5-dioxo-3-pyrrolidin-1-yl 4-[(2,5-dioxo-3-pyrrolin-1-yl)methyl]cyclohexanecarbox-ylate}, C 16 H 18 N 2 O 6 , crystallizes as discrete molecules separated by normal van der Waals interactions. The succinimide ester and maleimide subunits occupy equatorial positions on the cyclohexane ring.
📜 SIMILAR VOLUMES
The molecule of the title compound, C~16~H~18~O~4~, is non-planar and the pyran ring adopts a half-chair conformation. Intermolecular C—H...O hydrogen-bond contacts link the molecules in the crystal structure, forming dimers approximately parallel to (011).
In the title molecule, C 24 H 20 N 2 O 5 , the cyclohexene ring adopts a half-chair conformation. The molecular structure shows some intra-and intermolecular hydrogen bonds.