Gabapentin-lactumchloranilic acid (1/1)

3Citations
Citations of this article
6Readers
Mendeley users who have this article in their library.

Abstract

In the title compound, C9H15NO·C 6H2Cl2O4 [sytematic name: 2-azaspiro-[4.5]decan-3-onechloranilic acid (1/1)], the cyclo-hexane ring of the lactam molecule adopts a slightly distorted normal chair conformation and the five-membered 3-azaspiro ring is in a slightly distorted chair conformation. The dihedral angle between the least-squares planes of the cyclohexane and 3-azaspiro rings is 84.0 (3)°. In the crystal, the chloranilic acid mol-ecule and the gabapentin-lactum mol-ecules are held together by strong inter-molecular N-H⋯O and O-H⋯O hydrogen bonds with two bifurcated O acceptor atoms on the chloranilic acid mol-ecule and one on the gabapentin-lactum mol-ecule, each bonding with an inter-and intra-molecular hydrogen bond. The molecules are linked into chains parallel to (011) and propagating along the b axis.

Cite

CITATION STYLE

APA

Jasinski, J. P., Butcher, R. J., Hakim Al-Arique, Q. N. M., Yathirajan, H. S., & Narayana, B. (2010). Gabapentin-lactumchloranilic acid (1/1). Acta Crystallographica Section E: Structure Reports Online, 66(1). https://doi.org/10.1107/S1600536809053410

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free