organic compounds
The title compound, C10H17N2O+·H2PO4−, consists of a rilmenidine cation and a phosphate anion. In the solid state, the inversion-related phosphate anions are linked by O—HO hydrogen bonds to form a chain along the a axis. The cations are connected to the chain via N—HO hydrogen bonds.
organic compounds
The title compound, C14H18N2O2, which was obtained from an extended Biginelli reaction, contains a pyran ring with a chair conformation, a pyrimidine ring with a half-chair conformation and a benzene ring. The crystal structure is stabilized by an intermolecular hydrogen-bond network involving both NH groups and the carbonyl group.
organic compounds
The title compound, C17H22O3, which was synthesized by the condensation of cyclohexane-1,3-dione and n-valeraldehyde, includes a partially hydrogenated xanthene ring system. The molecule has crystallographic mirror symmetry. The central ring adopts a very shallow boat conformation while the symmetry-related outer six-membered rings have sofa conformations. Molecules form extended tapes in the c-axis direction though weak C—HO interactions.
organic compounds
The title compound, C14H18N2O2S, which was obtained from an extended Biginelli reaction, contains a pyran ring with a chair conformation, a pyrimidine ring with a half-chair conformation and a benzene ring. The crystal structure is stabilized by an intermolecular hydrogen-bond network.
organic compounds
The title compound, C30H48O2, is a triterpenoid which was isolated from the stalks of Celastrus hypoleucus (Oliv.) Warb. The molecule contains five six-membered rings adopting distorted boat, half-chair and chair conformations. The hydroxy groups serve as hydrogen-bond donors and the carbonyl groups as acceptors, forming molecular chains parallel to the b axis.