3-Fluoro-4-nitrophenyl 4-methylbenzenesulfonate
نویسندگان
چکیده
منابع مشابه
3-Fluoro-4-(4-hydroxyphenoxy)benzonitrile
The title compound, C(13)H(8)FNO(2), was synthesized from 3,4-difluoro-benzonitrile and hydro-quinone. The dihedral angle between the two aromatic rings is 70.9 (2)°. In the crystal structure, mol-ecules are linked by O-H⋯N hydrogen bonds, forming zigzag chains.
متن کامل3-Fluoro-4-nitrophenyl 4-methylbenzenesulfonate
In the title compound, C(13)H(10)FNO(5)S, the dihedral angle between the benzene rings is 47.63 (14)°. In the crystal, π-π stacking occurs between nearly parallel benzene rings of adjacent mol-ecules, the centroid-centroid distance being 3.7806 (16) Å. Weak inter-molecular C-H⋯O hydrogen bonding is also present in the crystal structure.
متن کاملTheoretical structural analysis of 3-CHLORO-4-FLUORO-ANILINE.
This study was designed to compute the spectroscopic properties of aniline family, and educates the 3chloro-4-fluoro-aniline, which have unique pharmaceutical important. The structural and spectroscopic properties were investigated using a quantum calculation. The density functional theory approach at B3LYP/6–31G(d) data set is apply. IR and UV-Visible spectrophotometric estimated through GAMES...
متن کاملEthyl 4-fluoro-3-nitrobenzoate
In the title compound, C(9)H(8)FNO(4), C-H⋯O inter-molecular inter-actions form dimers with R(2) (2)(10) motifs. These dimers are arranged into chains parallel to the b axis and the chains are stacked down the c axis.
متن کامل(4-Chlorobenzoyl)(4-chlorophenyl)amino 3-(2-nitrophenyl)propanoate
In the title hydroxamic acid derivate, C22H16Cl2N2O5, the nitro-substituted benzene ring forms dihedral angles of 14.11 (15) and 16.08 (15)°, with the 4-chloro-benzoyl and 4-chloro-phenyl benzene rings, respectively. The dihedral angle between the chloro-substituted benzene rings is 2.28 (13)°. In the crystal, mol-ecules are linked by weak C-H⋯O hydrogen bonds, forming chains along [100].
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ژورنال
عنوان ژورنال: Acta Crystallographica Section E Structure Reports Online
سال: 2011
ISSN: 1600-5368
DOI: 10.1107/s1600536811005903