Background: According to highlighted role of men in family planning, the use of reversible methods of contraception with no adverse effects on androgen-dependent metabolic reactions is very important. Therefore, in order to achieve a conductor combination in the designing contraceptive drugs, in the study, the effect of two drugs: Propylene glycol and Cyclo Hexyl on histological parameters of s...

The title compound, C(15)H(23)NO(2)S, contains cyclo-hexyl and ethyl substituents on the sulfonamide N atom and the cyclo-hexyl ring adopts a classic chair conformation. The dihedral angle between the benzene ring plane and the mean plane through the six atoms of the cyclo-hexyl ring is 59.92 (6)°. In the crystal structure, C-H⋯O hydrogen bonds link mol-ecules into sheets extending in the bc pl...

In the title compound, C(16)H(19)ClO(2)S, the cyclo-hexyl ring adopts a chair conformation and the aryl-sulfinyl unit is positioned equatorial relative to the cyclo-hexyl group. The least-squares plane through all six C atoms of the cyclo-hexyl ring makes a dihedral angle of 74.80 (6)° with the mean plane of the benzofuran fragment. In the crystal, mol-ecules are linked through inter-molecular ...

The title compound, C(15)H(23)NO(2)S, synthesized by N-methyl-ation of cyclo-hexyl-amine sulfonamide with propyl iodide, is of inter-est as a precursor to biologically active sulfur-containing heterocyclic compounds. The cyclo-hexyl ring exists in the chair form and the dihedral angle between the ring plane of the benzene ring and that of the cyclo-hexyl ring is 50.13 (9)°.

In the title complex, [Pt(C(6)H(11))Cl(C(8)H(12))], the Pt(II) ion lies in a distorted square-planar environment defined by the Cl and cyclo-hexyl C atoms and the mid-points of the two π-coordinated double bonds of cyclo-octa-1,5-diene. As a result of the different trans influences of the Cl atom and the cyclo-hexyl group, the Pt-C bonds trans to the cyclo-hexyl group are longer than those tran...

In the title solvated phosphonium salt, C34H40P(+)·Cl(-)·2CHCl3, the two cyclo-hexyl and two 1-naphthyl-methyl groups at the P atom are in a distorted tetra-hedral arrangement [105.26 (6)-113.35 (6)°]. Both cyclo-hexyl rings adopt a chair conformation. The dihedral angle between the naphthyl ring systems is 74.08 (3)°.

The title compound, C(16)H(25)NO(2)S, is a sulfonamide derivative with the substitution of propyl and cyclo-hexyl groups at the N atom. The least-squares plane through all six C atoms of the cyclo-hexyl ring forms a dihedral angle of 58.88 (12)° with the toluene ring. No hydrogen-bonding inter-actions are present in the crystal structure.

The title compound, C(13)H(15)BrClNO, was prepared by the condensation of equimolar quanti-ties of 3-bromo-5-chloro-salicyl-aldehyde with cyclo-hexyl-amine in methanol. There is an intra-molecular O-H⋯N hydrogen bond in the mol-ecule. The cyclo-hexyl ring adopts a chair conformation.

In the title compound, C(15)H(17)FO(3)S, the cyclo-hexyl ring adopts a classic chair conformation and the aryl-sulfonyl unit is positioned equatorial relative to the cyclo-hexyl group. In the crystal, mol-ecules are linked through weak inter-molecular C-H⋯O hydrogen bonds.

The title salt, C18H26N42+·2Cl-, was obtained by the protonation of N,N-bis-(pyridin-4-ylmeth-yl)cyclo-hexane-1,4-di-amine with hydro-chloric acid in ethanol. The asymmetric unit consists of one half of an N,N-bis-(pyridin-3-ylmeth-yl)cyclo-hexane-1,4-di-ammonium dication, with a crystallographic inversion centre located at the centre of the cyclo-hexyl ring, and a chloride anion. The central c...