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5-Ethyl-4a-meth-oxy-1,3-dimethyl-4a,5-dihydro-benzo[g]pteridine-2,4(1H,3H)dione.

Ménová P, Eigner V, Cibulka R, Cejka J, Dvořáková H - Acta Crystallogr Sect E Struct Rep Online (2009)

Bottom Line: The heterocyclic rings are substituted with methyl, ethyl and meth-oxy groups.The central tricyclic skeleton is bent due to the presence of an sp(3) C atom.There are weak inter-molecular C-H⋯O inter-actions in the structure, forming a three-dimensional network.

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ABSTRACT
The title compound, C(15)H(18)N(4)O(3), was formed by the reaction of methanol with 5-ethyl-1,3-dimethyl-alloxazinium perchlorate. Its structure mimics those of possible flavin inter-mediates in flavoenzymes. The heterocyclic rings are substituted with methyl, ethyl and meth-oxy groups. The central tricyclic skeleton is bent due to the presence of an sp(3) C atom. There are weak inter-molecular C-H⋯O inter-actions in the structure, forming a three-dimensional network.

No MeSH data available.


Related in: MedlinePlus

Formation of the adduct by the reaction of 5-ethyl-1,3-dimethylalloxazinium perchlorate with methanol.
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Fap2: Formation of the adduct by the reaction of 5-ethyl-1,3-dimethylalloxazinium perchlorate with methanol.


5-Ethyl-4a-meth-oxy-1,3-dimethyl-4a,5-dihydro-benzo[g]pteridine-2,4(1H,3H)dione.

Ménová P, Eigner V, Cibulka R, Cejka J, Dvořáková H - Acta Crystallogr Sect E Struct Rep Online (2009)

Formation of the adduct by the reaction of 5-ethyl-1,3-dimethylalloxazinium perchlorate with methanol.
© Copyright Policy - open-access
Related In: Results  -  Collection

License
Show All Figures
getmorefigures.php?uid=PMC2969355&req=5

Fap2: Formation of the adduct by the reaction of 5-ethyl-1,3-dimethylalloxazinium perchlorate with methanol.
Bottom Line: The heterocyclic rings are substituted with methyl, ethyl and meth-oxy groups.The central tricyclic skeleton is bent due to the presence of an sp(3) C atom.There are weak inter-molecular C-H⋯O inter-actions in the structure, forming a three-dimensional network.

View Article: PubMed Central - HTML - PubMed

ABSTRACT
The title compound, C(15)H(18)N(4)O(3), was formed by the reaction of methanol with 5-ethyl-1,3-dimethyl-alloxazinium perchlorate. Its structure mimics those of possible flavin inter-mediates in flavoenzymes. The heterocyclic rings are substituted with methyl, ethyl and meth-oxy groups. The central tricyclic skeleton is bent due to the presence of an sp(3) C atom. There are weak inter-molecular C-H⋯O inter-actions in the structure, forming a three-dimensional network.

No MeSH data available.


Related in: MedlinePlus