The asymmetric unit of the title co-crystal, 2CH(4)N(2)O·C(6)H(10)O(4), contains two urea mol-ecules and two half-mol-ecules of adipic acid; the latter are completed by crystallographic inversion symmetry. The crystal packing is stabilized by O-H⋯O and N-H⋯O hydrogen bonds, generating a chain along [110]. Additional weak inter-chain O-H⋯O and N-H⋯O inter-molecular inter-actions lead to the form...

In the title compound, C(20)H(28)N(4) (2+)·2PF(6) (-), the dihedral angles between the benzene ring and the imidazole rings are 70.18 (11) and 69.83 (11)°, while the imidazole rings form a dihedral angle of 40.52 (12)°. In the crystal, weak C-H⋯F inter-actions link the mol-ecules into a two-dimensional network parallel to (001). A π-π inter-action with a centroid-centroid distance of 3.601 (1) ...

The title compound, C(5)H(8)ClNO(3), was prepared by the nucleophilic substitution reaction of (2S)-2-chloro-propanoyl chloride with glycine. The acetate group forms a dihedral angle of 84.6 (1)° with the mean plane of the C-NH-C=O fragment. In the crystal, the molecules are linked by N-H⋯O and O-H⋯O hydrogen bonds, generating a three-dimensional network, which consolidates the crystal packing.

In the title molecular salt, C(7)H(20)N(2) (2+)·2NO(3) (-), the crystal structure exhibits an unusual back-to-back paired double-stacked packing arrangement culminating in an overall double zigzag pattern of the dications. The nitrate anions form a ring around one pair of double-stacked dications. An intricate three-dimensional N-H⋯O and N-H⋯(O,O) hydrogen-bonding network exists in the crystal ...

The crystal structure of the title compound, K+.C6H4NO6S-, is built up from p-nitrophenyl sulfate anions and potassium cations. Adjacent anions form dimers, which are linked together in a three-dimensional network via short C-H...O contacts. The coordination sphere of the K+ ions may be described as a distorted square antiprism. The crystal structure is further stabilized by pi-pi stacking inte...

The title compound, C(16)H(16)O(8), is a potent nonspecific phyto-toxin. The crystal structure is the average of two tauto-mers, 5,6,7,9,10-penta-hydr-oxy-2-meth-oxy-7-methyl-1,4,5,6,7,8-hexa-hydro-anthracene-1,4-dione and 1,4,5,6,7-pentahydr-oxy-2-meth--oxy-7-methyl-5,6,7,8,9,10-hexa-hydro-anthracene-9,10-di-one. The cyclo-hexene rings in both tautomers display a half-chair conformation. An ex...

The crystal packing of the title compound, C(6)H(11)N(2)O(+)·I(-), can be described as inter-calated layers lying parallel to (010), with the iodide ions located between the cations. A weak intra-molecular C-H⋯O hydrogen bond occurs within the cation. In the crystal, inter-molecular O-H⋯I hydrogen bonds result in the formation of a three-dimensional network and reinforce the cohesion of the ion...

The asymmetric unit of the title compound, C(5)H(9)N(3) (2+)·2Cl(-), contains two diprotonated 2,3-diamino-pyridine cations and four chloride anions. In the crystal structure, the anions and cations are connected by inter-molecular N-H⋯Cl and C-H⋯Cl hydrogen bonds, forming a three-dimensional network. The crystal structure is further stabilized by π-π inter-actions between pyridinium rings [cen...

The conformation adopted by the title compound, C20H21N3O3, in the crystal is 'J'-shaped and appears to be at least partially directed by a weak intra-molecular C-H⋯N hydrogen bond. In the crystal, mol-ecules are linked by N-H⋯O hydrogen bonds, forming dimers with R 2 (2)(8) motifs. Furthermore, these dimers connect to each other via C-H⋯O and N-H⋯O hydrogen bonds to form a three-dimensional ne...

The title compound, C15H17NO4, containing two mol-ecules in the asymmetric unit is a polymorph of the crystal structure published by Martínez et al. [(2011). Eur. J. Org. Chem. pp. 3137-3145] which at 120 K is monoclinic with one mol-ecule in the asymmetric unit. Both mol-ecules in the title compound are in the trans form. In the crystal, N-H⋯O and O-H⋯O hydrogen bonds connect mol-ecules, formi...