3-(Pyridin-3-yl)propionic acid

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منابع مشابه

3-(Pyridin-3-yl)propionic acid

In the crystal of the title compound, C(8)H(9)NO(2), mol-ecules assemble to form C(8) chains along the b axis by N-H⋯O hydrogen bonds, supported by weaker C-H⋯O hydrogen bonded-inter-actions between adjacent chains.

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3-[3-(Pyridin-3-yl)-1,2,4-oxadiazol-5-yl]propanoic acid

In the title compound, C(10)H(9)N(3)O(3), the benzene ring is almost coplanar with the heterocyclic ring, making a dihedral angle of 11.3 (1)°. The plane of the carboxyl group is rotated by 8.4 (2)° with respect to the 1,2,4-oxadiazole ring plane. The aliphatic chain exhibits an extended conformation. In the crystal, mol-ecules are liked through inter-molecular O-H⋯N bonds, forming a chain stru...

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3-[(E)-(Pyridin-3-yl­imino)­meth­yl]phenol

Two independent mol-ecules are present in the asymmetric unit of the title compound, C(12)H(10)N(2)O, in which the 3-hy-droxy-benzaldehyde and the pyridin-3-amine units are almost planar [r.m.s. deviations of 0.0236 and 0.0116Å, respectively, in one mol-ecule and 0.0245 and 0.0162Å, respectively, in the other] and are oriented at dihedral angles of 7.21 (7) and 14.77 (7)°. In the crystal, mol-e...

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4-({[(E)-Pyridin-3-yl­methyl­idene]amino}­meth­yl)cyclo­hexa­necarb­oxy­lic acid

The title compound, C(14)H(18)N(2)O(2), contains two geometrically different mol-ecules in the asymmetric unit: the basal plane of the cyclo-hexane chair and the N-[pyridin-3-yl-methyl-idene]methanamine moiety are oriented at dihedral angles of 71.77 (7)° and 83.42 (8)°. In the crystal, the mol-ecules are linked by O-H⋯N hydrogen bonds, generating C(13) head-to-tail chains extending along the b...

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3-(Pyridin-4-ylmeth­oxy)phenol

In the title compound, C(12)H(11)NO(2), the phenolic ring is inclined at an angle of 32.70 (1)° with respect to the pyridine ring. In the crystal, inter-molecular O-H⋯N hydrogen bonds link the mol-ecules into C(11) chains along [001].

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ژورنال

عنوان ژورنال: Acta Crystallographica Section E Structure Reports Online

سال: 2010

ISSN: 1600-5368

DOI: 10.1107/s1600536810052384