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5-[3-(2,5-Dimethoxy-phen-yl)prop-2-enyl-idene]-1,3-diethyl-2-thioxohexa-hydro-pyrimidine-4,6-dione.

Asiri AM, Khan SA, Ng SW - Acta Crystallogr Sect E Struct Rep Online (2009)

Bottom Line: 1,3-Diethyl-2-thio-barbituric acid reacts with 2,5-dimethoxy-benzaldehyde to form the title Knoevenagel product, C(19)H(22)N(2)O(4)S.In the compound, the two six-membered rings at either end of the three-membered -CHCHCH- chain are nearly coplanar with this fragment (r.m.s. deviation of the two six-membered rings and the three chain atoms = 0.08 Å).

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ABSTRACT
1,3-Diethyl-2-thio-barbituric acid reacts with 2,5-dimethoxy-benzaldehyde to form the title Knoevenagel product, C(19)H(22)N(2)O(4)S. In the compound, the two six-membered rings at either end of the three-membered -CHCHCH- chain are nearly coplanar with this fragment (r.m.s. deviation of the two six-membered rings and the three chain atoms = 0.08 Å).

No MeSH data available.


Thermal ellipsoid plot (Barbour, 2001) of C19H22N2O4S at the 70% probability level; hydrogen atoms are drawn as spheres of arbitrary radius.
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Fap1: Thermal ellipsoid plot (Barbour, 2001) of C19H22N2O4S at the 70% probability level; hydrogen atoms are drawn as spheres of arbitrary radius.


5-[3-(2,5-Dimethoxy-phen-yl)prop-2-enyl-idene]-1,3-diethyl-2-thioxohexa-hydro-pyrimidine-4,6-dione.

Asiri AM, Khan SA, Ng SW - Acta Crystallogr Sect E Struct Rep Online (2009)

Thermal ellipsoid plot (Barbour, 2001) of C19H22N2O4S at the 70% probability level; hydrogen atoms are drawn as spheres of arbitrary radius.
© Copyright Policy - open-access
Related In: Results  -  Collection

License
Show All Figures
getmorefigures.php?uid=PMC2977468&req=5

Fap1: Thermal ellipsoid plot (Barbour, 2001) of C19H22N2O4S at the 70% probability level; hydrogen atoms are drawn as spheres of arbitrary radius.
Bottom Line: 1,3-Diethyl-2-thio-barbituric acid reacts with 2,5-dimethoxy-benzaldehyde to form the title Knoevenagel product, C(19)H(22)N(2)O(4)S.In the compound, the two six-membered rings at either end of the three-membered -CHCHCH- chain are nearly coplanar with this fragment (r.m.s. deviation of the two six-membered rings and the three chain atoms = 0.08 Å).

View Article: PubMed Central - HTML - PubMed

ABSTRACT
1,3-Diethyl-2-thio-barbituric acid reacts with 2,5-dimethoxy-benzaldehyde to form the title Knoevenagel product, C(19)H(22)N(2)O(4)S. In the compound, the two six-membered rings at either end of the three-membered -CHCHCH- chain are nearly coplanar with this fragment (r.m.s. deviation of the two six-membered rings and the three chain atoms = 0.08 Å).

No MeSH data available.