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l-Nebiviololinium chloride dihydrate.

Tuchalski G, Hänsicke A, Reck G, Emmerling F - Acta Crystallogr Sect E Struct Rep Online (2007)

Bottom Line: The hydro-chloride salt of chiral l-nebivolol {systematic name: (+)-(R,S,S,S)-bis-[2-(6-fluoro-3,4-dihydro-2H-1-benzopyran-2-yl)-2-hydroxy-ethyl]ammonium chloride dihydrate}, C(22)H(26)F(2)NO(4) (+)·Cl(-)·2H(2)O, was obtained by chiral liquid chromatography as a dihydrate.The pyran rings adopt half-chair conformations.Hydrogen bonds between the cation, anions and water mol-ecules contribute to the formation of layers parallel to the ac plane.

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ABSTRACT
The hydro-chloride salt of chiral l-nebivolol {systematic name: (+)-(R,S,S,S)-bis-[2-(6-fluoro-3,4-dihydro-2H-1-benzopyran-2-yl)-2-hydroxy-ethyl]ammonium chloride dihydrate}, C(22)H(26)F(2)NO(4) (+)·Cl(-)·2H(2)O, was obtained by chiral liquid chromatography as a dihydrate. The pyran rings adopt half-chair conformations. Hydrogen bonds between the cation, anions and water mol-ecules contribute to the formation of layers parallel to the ac plane.

No MeSH data available.


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View of the layers array of (I), formed via hydrogen-bonding interactions (indicated by green lines).
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Fap2: View of the layers array of (I), formed via hydrogen-bonding interactions (indicated by green lines).


l-Nebiviololinium chloride dihydrate.

Tuchalski G, Hänsicke A, Reck G, Emmerling F - Acta Crystallogr Sect E Struct Rep Online (2007)

View of the layers array of (I), formed via hydrogen-bonding interactions (indicated by green lines).
© Copyright Policy - open-access
Related In: Results  -  Collection

License
Show All Figures
getmorefigures.php?uid=PMC2915012&req=5

Fap2: View of the layers array of (I), formed via hydrogen-bonding interactions (indicated by green lines).
Bottom Line: The hydro-chloride salt of chiral l-nebivolol {systematic name: (+)-(R,S,S,S)-bis-[2-(6-fluoro-3,4-dihydro-2H-1-benzopyran-2-yl)-2-hydroxy-ethyl]ammonium chloride dihydrate}, C(22)H(26)F(2)NO(4) (+)·Cl(-)·2H(2)O, was obtained by chiral liquid chromatography as a dihydrate.The pyran rings adopt half-chair conformations.Hydrogen bonds between the cation, anions and water mol-ecules contribute to the formation of layers parallel to the ac plane.

View Article: PubMed Central - HTML - PubMed

ABSTRACT
The hydro-chloride salt of chiral l-nebivolol {systematic name: (+)-(R,S,S,S)-bis-[2-(6-fluoro-3,4-dihydro-2H-1-benzopyran-2-yl)-2-hydroxy-ethyl]ammonium chloride dihydrate}, C(22)H(26)F(2)NO(4) (+)·Cl(-)·2H(2)O, was obtained by chiral liquid chromatography as a dihydrate. The pyran rings adopt half-chair conformations. Hydrogen bonds between the cation, anions and water mol-ecules contribute to the formation of layers parallel to the ac plane.

No MeSH data available.


Related in: MedlinePlus