In the title molecule, C~21~H~31~ClO~4~, rings __A__, __B__ and __C__ have regular chair conformations, while ring __D__ has an envelope form. In the crystal structure, weak intermolecular C—H...O hydrogen bonds link the molecules into zigzag chains running along the __b__ axis.
3β-Acetoxy-5α-chloro-6β-hydroxyandrostan-17-one
✍ Scribed by Xia, Chun-Nian ;Li, Bi-Wen ;Hu, Wei-xiao ;Zhou, Wei
- Publisher
- International Union of Crystallography
- Year
- 2007
- Tongue
- English
- Weight
- 396 KB
- Volume
- 63
- Category
- Article
- ISSN
- 1600-5368
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✦ Synopsis
The title compound, C 21 H 31 ClO 4 , crystallizes with two molecules in the asymmetric unit. Rings A, B and C have chair conformations, while ring D has an envelope form. The crystal packing shows that the molecules are connected by intermolecular O-HÁ Á ÁO hydrogen bonds.
📜 SIMILAR VOLUMES
In the title molecule, C 22 H 29 ClO 4 , all bond lengths and angles show normal values. Rings A and C have slightly distorted chair conformations, while rings B and D show envelope conformations. Weak intermolecular C-HÁ Á ÁO hydrogen bonds link the molecules into chains running along the b axis.
In the crystal structure of the title compound, C 22 H 30 O 4 , rings A and C have slightly distorted chair conformations, ring B shows an approximate symmetric half-chair conformation and ring D is in an envelope conformation. The molecules are connected by weak intermolecular C-HÁ Á ÁO hydrogen bo
The structure of the title compound, C 22 H 28 O 5 , which is a natural furan diterpene, has been determined. The crystal structure is stabilized by CÐHÁ Á ÁO intermolecular interactions.