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2-Amino-4,6-dimethyl-pyrimidine-anthranilic acid (1/1).

Ebenezer S, Muthiah PT - Acta Crystallogr Sect E Struct Rep Online (2010)

Bottom Line: One of them is formed by the inter-action of 2-amino-4,6-dimethyl-pyrimidine (AMPY) with the carboxyl group of anthranilic acid (AA) through N-H⋯O and O-H⋯N hydrogen bonds, whereas the other is formed through the inter-action of two centrosymmetrically related pyrimidines involving N-H⋯N hydrogen bonds.These two combined motifs form a heterotetra-mer.The heterotetra-mer sheets are stacked into three-dimensional network.

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Affiliation: School of Chemistry, Bharathidasan University, Tiruchirappalli 620 024, Tamilnadu, India.

ABSTRACT
In the title 1:1 adduct, C(6)H(9)N(3)·C(7)H(7)NO(2), the crystal structure is stabilized by hydrogen bonds involving two different R(2) (2)(8) motifs. One of them is formed by the inter-action of 2-amino-4,6-dimethyl-pyrimidine (AMPY) with the carboxyl group of anthranilic acid (AA) through N-H⋯O and O-H⋯N hydrogen bonds, whereas the other is formed through the inter-action of two centrosymmetrically related pyrimidines involving N-H⋯N hydrogen bonds. These two combined motifs form a heterotetra-mer. The heterotetra-mer sheets are stacked into three-dimensional network.

No MeSH data available.


ORTEP view of the title compound showing the 50% probability displacement ellipsoids. Dashed lines indicate hydrogen bonds.
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Fap1: ORTEP view of the title compound showing the 50% probability displacement ellipsoids. Dashed lines indicate hydrogen bonds.


2-Amino-4,6-dimethyl-pyrimidine-anthranilic acid (1/1).

Ebenezer S, Muthiah PT - Acta Crystallogr Sect E Struct Rep Online (2010)

ORTEP view of the title compound showing the 50% probability displacement ellipsoids. Dashed lines indicate hydrogen bonds.
© Copyright Policy - open-access
Related In: Results  -  Collection

License
Show All Figures
getmorefigures.php?uid=PMC2983637&req=5

Fap1: ORTEP view of the title compound showing the 50% probability displacement ellipsoids. Dashed lines indicate hydrogen bonds.
Bottom Line: One of them is formed by the inter-action of 2-amino-4,6-dimethyl-pyrimidine (AMPY) with the carboxyl group of anthranilic acid (AA) through N-H⋯O and O-H⋯N hydrogen bonds, whereas the other is formed through the inter-action of two centrosymmetrically related pyrimidines involving N-H⋯N hydrogen bonds.These two combined motifs form a heterotetra-mer.The heterotetra-mer sheets are stacked into three-dimensional network.

View Article: PubMed Central - HTML - PubMed

Affiliation: School of Chemistry, Bharathidasan University, Tiruchirappalli 620 024, Tamilnadu, India.

ABSTRACT
In the title 1:1 adduct, C(6)H(9)N(3)·C(7)H(7)NO(2), the crystal structure is stabilized by hydrogen bonds involving two different R(2) (2)(8) motifs. One of them is formed by the inter-action of 2-amino-4,6-dimethyl-pyrimidine (AMPY) with the carboxyl group of anthranilic acid (AA) through N-H⋯O and O-H⋯N hydrogen bonds, whereas the other is formed through the inter-action of two centrosymmetrically related pyrimidines involving N-H⋯N hydrogen bonds. These two combined motifs form a heterotetra-mer. The heterotetra-mer sheets are stacked into three-dimensional network.

No MeSH data available.