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5-Hydr­oxy-7-meth­oxy-2-(4-methoxy­phen­yl)-4H-1-benzopyran-4-one. Corrigendum

✍ Scribed by Teh, Jeannie Bee-Jan ;Fun, Hoong-Kun ;Razak, Ibrahim Abdul ;Chantrapromma, Suchada ;Boonnak, Nawong ;Karalai, Chatchanok


Publisher
International Union of Crystallography
Year
2005
Tongue
English
Weight
37 KB
Volume
61
Category
Article
ISSN
1600-5368

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5-Hydr­oxy-7-meth­oxy-2-(4-methoxy­phen­
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The title compound, C 17 H 14 O 5 , a flavone, was isolated from the rhizomes of Kaempferia parviflora. The benzopyran-4-one ring system and the methoxyphenyl substituent are approximately coplanar. The molecules are linked via intermolecular C-HÁ Á ÁO hydrogen bonds to form chains.

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The title compound, C 17 H 14 O 5 , a flavone, was isolated from the rhizomes of Kaempferia parviflora. There are two crystallographically independent molecules in the asymmetric unit. The molecular structure is stabilized by intramolecular O-HÁ Á ÁO and C-HÁ Á ÁO hydrogen bonds. C-HÁ Á ÁO intermole

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In the title compound, C 16 H 13 ClN 2 O 2 , the dihedral angle between the pyridine and benzene rings is 40.1 (1) . There is a weak intramolecular C-HÁ Á ÁCl interaction. Molecules are linked via O-HÁ Á ÁN hydrogen bonds, forming chains of graph-set motif C(6) along the a axis.

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The title compound, C 13 H 14 O 4 , known as 8-methyleugenitin, is a chromone isolated from the leaves of Mellaleuca cajuputi Powell. The chromone unit is essentially planar. The methyl and hydroxyl groups lie in the plane of the benzene ring while the methoxy substituent is perpendicular to it. An