3-(7-Methoxy-β-carbolin-1-yl)propionic acid monohydrate
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چکیده
منابع مشابه
3-(7-Methoxy-β-carbolin-1-yl)propionic acid monohydrate
In the title compound, C(15)H(14)N(2)O(3)·H(2)O [systematic name: 3-(7-meth-oxy-9H-pyrido[3,4-b]indol-1-yl)propanoic acid monohydrate], the fused rings make dhedral angles of 0.4 (1), 1.1 (2) and 1.4 (2)°. In the crystal, the water mol-ecule is involved in the formation of three independent hydrogen-bonded chains via O-H⋯O and N-H⋯O hydrogen bonds, while the carb-oxy group forms an inter-molecu...
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In the title compound, C(24)H(18)N(2)O(4), the phenyl and benzene rings are both oriented almost perpendicular to the naphthalene ring system at dihedral angles of 70.97 (5) and 84.64 (5)°. The former rings make a dihedral angle of 87.15 (6)°. The mol-ecule has a Z configuration about the C=N bond. In the crystal, mol-ecules are connected by a pair of inter-molecular O-H⋯O hydrogen bonds betwee...
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The mol-ecule of accanthomine A, C(15)H(13)N(5), is approximately planar, with the indolyl fused-ring and the pyrimidyl ring being twisted by 31.7 (1)° The amino group of the five-membered ring is an intramolecular hydrogen-bond donor to a nitro-gen acceptor of the pyrimide ring. The amino group of the pyrimide ring is a hydrogen-bond donor to the N atoms of adjacent mol-ecules. These hydrogen-...
متن کامل3-Aminophenylboronic acid monohydrate
In the title compound, C(6)H(8)BNO(2)·H(2)O, the almost planar boronic acid mol-ecules (r.m.s. deviation = 0.044 Å) form inversion dimers, linked by pairs of O-H⋯O hydrogen bonds. The water mol-ecules link these dimers into [100] chains by way of O-H⋯O hydrogen bonds, and N-H⋯O links generate (100) sheets.
متن کامل3-Phenyl-2-(1H-tetrazol-1-yl)propanoic acid monohydrate
In the title compound, C(10)H(10)N(4)O(2)·H(2)O, the dihedral angle between the tetra-zole and benzene rings is 63.24 (11)°. The crystal structure is stabilized by intra-molecular O-H⋯N and O-H⋯O hydrogen bonds.
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ژورنال
عنوان ژورنال: Acta Crystallographica Section E Structure Reports Online
سال: 2011
ISSN: 1600-5368
DOI: 10.1107/s160053681101350x