In the title compound, C14H16ClNO2, the cyclo-hexyl ring has a chair conformation. The dihedral angle between the benzene ring and the mean plane of the four planar C atoms of the cyclo-hexyl ring is 45.2 (3)°. The two carbonyl groups are trans to one another, with an O=C-C=O torsion angle of -137.1 (3)°. In the crystal, mol-ecules are linked by N-H⋯O hydrogen bonds forming chains propagating a...

In the title mol-ecule, C15H20N4OS2, the acetamido fragment is nearly coplanar with the pyridyl ring [C-N-C-C torsion angle = -4.1 (2)°], while the cyclo-hexyl-sulfanyl portion protrudes from this plane [N-C-C-S torsion angle = -40.8 (6)°]. In the crystal, alternating pairwise N-H⋯O and N-H⋯N hydrogen bonds across inversion centres form chains along [101], which are associated into stepped laye...

In the cation of the title compound, C16H26NO2 (+)·C6HCl2O4 (-)·C4H8O2, the 1-hy-droxy-cyclo-hexyl ring adopts a slightly distorted chair conformation. The dihedral angle between the mean planes of the 1-hy-droxy-cyclo-hexyl and 4-hy-droxy-phenyl rings is 84.0 (8)°. In the anion, the hydroxyl H atom is twisted slightly out of the ring plane with a C-C-O-H torsion angle of -171.9°. Disorder was ...

The mol-ecular and crystal structures of the title compound, C(23)H(28)Cl(2)N(2)O(2), are very close to those of the bromine-substituted analogue N,N-dicyclo-hexyl-2-(5,7-dibromo-8-quinol-yloxy)acetamide. The two cyclo-hexyl groups adopt normal chair conformation. The amide N and C atoms have a planar configuration. The crystal packing is stabilized by inter-molecular C-H⋯O hydrogen bonds and a...

The title compound, a Ga(II) dimer, [Ga(2)Br(4)(C(12)H(23)P)(2)], was synthesized by reaction of GaBr(THF)(n) (THF is tetra-hydro-furan) with dicyclo-hexyl-phosphine in toluene. At 150 K the crystallographically centrosymmetric molecule exhibits disorder in which one of the two independent cyclo-hexyl groups is modelled over two sites in a 62 (1):38 (1) ratio. In d(6)-benzene solution, the comp...

Two ytterbium(III) complexes comprising alkynylamidinate ligands, namely bis-(η5-cyclo-penta-dien-yl)(3-cyclo-propyl-N,N'-diiso-propyl-propynamidinato-κ2N,N')ytterbium(III), [Yb(C5H5)2(C12H19N2)] or Cp2Yb[( i Pr2N)2C-C≡C-c-C3H5] (1) and tris-(3-phenyl-N,N'-di-cyclo-hexyl-propynamidinato-κ2N,N')ytterbium(III), [Yb(C21H27N2)3] or Yb[(CyN)2C-C≡C-Ph]3 (Cy = cyclo-hex-yl) (2) have been synthesized a...

In the title compound, C(21)H(21)FO(2)S, the cyclo-hexyl ring adopts a classic chair conformation. The 4-fluoro-phenyl ring makes a dihedral angle of 31.05 (6)° with the mean plane of the benzofuran fragment. In the crystal, mol-ecules are linked through weak inter-molecular C-H⋯O and C-H⋯π inter-actions.

In the title compound, C(21)H(21)FO(3)S, the cyclo-hexyl ring adopts a chair conformation. The 3-fluoro-phenyl ring makes a dihedral angle of 79.15 (4)° with the mean plane of the benzofuran fragment. In the crystal, mol-ecules are linked by weak inter-molecular C-H⋯O hydrogen bonds and C-H⋯π inter-actions.

The title compound, C(12)H(16)ClNO(2)S, adopts an L-shaped conformation, with the central C-S-N-C torsion angle being -78.0 (2)°. The cyclo-hexyl ring adopts a chair conformation. In the crystal, adjacent mol-ecules are connected by pairs of N-H⋯O hydrogen bonds around an inversion centre, forming cyclic dimers [graph set R(2) (2)(8)].

In the title compound, C(13)H(17)NO(2), the dihedral angle between the benzene ring and the basal plane of the cyclo-hexyl ring is 49.55 (8)°. In the crystal, mol-ecules are linked by N-H⋯O hydrogen bonds, forming chains propagating in [010].