3-Nitro-2-phenylchroman

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منابع مشابه

3-Nitro-2-phenyl­chroman

In the title compound, C(15)H(13)NO(3), the dihedral angle between the two aromatic rings is 79.25 (16)°.

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4-Oxo-2-phenylchroman-6-yl propionate

In the structure of the title compound, C(18)H(16)O(4), both the S and R enanti-omers appear to occupy in a random way four symmetry-equivalent sites of the unit cell in an approximately 4:1/1:4 ratio. The chiral C atom of the pyrone ring together with the phenyl ring bonded to this atom are disordered over two positions, the occupancy factor of the major component being 0.809 (5). Adjacent mol...

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2-Hydr­oxy-3-nitro-N-phenyl­benzamide

The asymmetric unit of the title compound, C(13)H(10)N(2)O(4), contains two crystallographically independent mol-ecules. The aromatic rings are oriented at dihedral angles of 24.39 (3) and 7.47 (3)° in the two mol-ecules and intra-molecular N-H⋯O and O-H⋯O hydrogen bonds result in the formation of two planar six-membered rings. In the crystal structure, inter-molecular O-H⋯O and C-H⋯O hydrogen ...

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2-Ferrocenyl-3-nitro-2H-chromene

In the title compound, [Fe(C5H5)(C14H10NO3)], the cyclo-penta-dienyl rings are in an eclipsed conformation and the pyran ring adopts a half-chair conformation. The mean plane of the pyran ring makes dihedral angles of 79.33 (1) and 80.73 (1)°, respectively, with the substituted and unsubstituted cyclo-penta-dienyl rings. In the crystal, pairs of C-H⋯O hydrogen bonds link the mol-ecules into inv...

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4-Formyl-2-nitro­phenyl 3-nitro-2-methyl­benzoate

In the title formyl nitro aryl benzoate derivative, C15H10N2O7, the benzene rings form a dihedral angle of 4.96 (3)°. The mean plane of the central ester group, C-O-C-(=O)-C (r.m.s. deviation = 0.0484 Å), is twisted away from the formyl nitro aryl and benzoate rings by 46.61 (5) and 49.93 (5)°, respectively. In the crystal, the mol-ecules are packed forming C-H⋯O inter-actions in chains which p...

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ژورنال

عنوان ژورنال: Acta Crystallographica Section E Structure Reports Online

سال: 2012

ISSN: 1600-5368

DOI: 10.1107/s1600536812020806