منابع مشابه
3-Benzoyl-5-chlorouracil
THE DIHEDRAL ANGLE BETWEEN THE PLANES OF TWO AROMATIC RINGS IN THE TITLE COMPOUND [SYSTEMATIC NAME: 3-benzoyl-5-chloro-pyrimidine-2,4(1H,3H)-dione], C(11)H(7)ClN(2)O(3), is 86.79 (6)°. Centrosymmetric dimers formed by N-H⋯O hydrogen bonds are linked through C-H⋯O inter-actions, forming a two-dimensional network parallel to (10).
متن کاملN-Benzoyl-3-nitrobenzenesulfonamide
In the title compound, C(13)H(10)N(2)O(5)S, the dihedral angle between the phenyl and benzene rings is 86.7 (1)°. In the crystal, mol-ecules are linked into zigzag C(4) chains running along the b axis via N-H⋯O hydrogen bonds.
متن کامل3-Benzoyl-1,1-dibenzylthiourea
Two independent thio-urea mol-ecules comprise the asymmetric unit of the title compound, C(22)H(20)N(2)OS. The central N-C(=S)N(H)C(=O) atoms in each mol-ecule are virtually superimposable and each is twisted [C-N-C-S torsion angles = 121.3 (3) and -62.3 (4)°]. The mol-ecules differ only in terms of the relative orientations of the benzyl benzene rings [major difference between the C-N-C-C tors...
متن کامل1-Benzoyl-3-ethyl-3-phenylthiourea
In the title compound, C(16)H(16)N(2)OS, the conformation at the two partially double C-N bonds of the thio-urea unit is E. The amide group is twisted relative to the thio-urea fragment, forming a dihedral angle of 62.44 (16)°, and the two phenyl rings form a dihedral angle 75.93 (18)°. In the crystal, mol-ecules are linked by N-H⋯S hydrogen bonds, forming centrosymmetric dimers.
متن کامل1-Benzoyl-3-methyl-3-pentylthiourea
Two independent mol-ecules comprise the asymmetric unit of the title compound, C(14)H(20)N(2)OS. These differ in the relative orientations of the pentyl chains [C-C-C-C torsion angles = -176.7 (3) and 176.4 (3)°]. Significant twists are evident in each mol-ecule, the dihedral angles formed between the thio-urea and amide residues being 53.47 (17) and 55.81 (17)°. In the crystal, each mol-ecule ...
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ژورنال
عنوان ژورنال: Acta Crystallographica Section E Structure Reports Online
سال: 2010
ISSN: 1600-5368
DOI: 10.1107/s1600536810036226