منابع مشابه
Butallylonal 1,4-dioxane hemisolvate
THE ASYMMETRIC UNIT OF THE TITLE COMPOUND [SYSTEMATIC NAME: 5-(1-bromo-prop-2-en-1-yl)-5-sec-butyl-pyrimidine-2,4,6-trione 1,4-dioxane hemisolvate], C(11)H(15)BrN(2)O(3)·0.5C(4)H(8)O(2), contains one half-mol-ecule of 1,4-dioxane and one mol-ecule of butallyl-onal, with an almost planar barbiturate ring [largest deviation from the mean plane = 0.049 (5) Å]. The centrosymmetric dioxane mol-ecule...
متن کاملCytenamide–1,4-dioxane (2/1)
IN THE CRYSTAL STRUCTURE OF THE TITLE COMPOUND [SYSTEMATIC NAME: 5H-dibenzo[a,d]cyclo-hepta-triene-5-carboxamide-1,4-dioxane (2/1)], 2C(16)H(13)NO·C(4)H(8)O(2), the cytenamide mol-ecules form a hydrogen-bonded R(2) (2)(8) dimer. The solvent mol-ecule is located between two adjacent cytenamide dimers and forms N-H⋯O hydrogen bonds with one cytenamide mol-ecule from each dimer.
متن کامل4-Hydroxybenzamide 1,4-dioxane hemisolvate
The asymmetric unit of the title compound, C(7)H(7)NO(2)·0.5C(4)H(8)O(2), is composed of one 4-hy-droxy-benzamide mol-ecule and half of a 1,4-dioxane mol-ecule. The complete dioxin molecule is generated by crystallographic inversion symmetry. The crystal has an extensive system of hydrogen bonds, in which the three donor H atoms are fully utilized: these result in amide-amide homodimers, and N-...
متن کامل2-(2-Naphthyl)-1,3-dioxane
The title compound, C(14)H(14)O(2), crystallizes in the chiral monoclinic space group P2(1). This acetal is composed of a planar naphthalene ring with a 1,3-dioxane ring substituent, which has a chair conformation. In the crystal structure, symmetry-related mol-ecules are connected via a weak C-H⋯O inter-action to form a helical chain propagating in [010]. While there are no π-π stacking inter-...
متن کامل2-Ethyl-5-triphenylmethyl-1,3-dioxane
In the title compound, C(25)H(26)O(2), the dioxane ring adopts a chair conformation with the two substituent groups occupying equatorial positions.
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ژورنال
عنوان ژورنال: Acta Crystallographica Section E Structure Reports Online
سال: 2005
ISSN: 1600-5368
DOI: 10.1107/s1600536805022464