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1-(3-Chloro-phen-yl)-5-(2,4-di-hydroxy-benzo-yl)pyridin-2(1H)-one.

1-(3-クロロフェニル)-5-(2,4-ジヒドロキシベンゾイル)ピリジン-2(1H)-オンの結晶構造解析

other not specified not assessed

Abstract

This study reports the X-ray crystal structure of the compound C18H12ClNO4. The chlorophenyl substituent exhibits positional disorder across two orientations, with site occupancies of 0.331(8) and 0.669(8). An intramolecular hydrogen bond is observed between a hydroxyl group and the acyclic carbonyl moiety. Within the crystal lattice, intermolecular O-H···O and C-H···O hydrogen bonding interactions link molecules into extended chains propagating along the [110] direction, generating a characteristic ladder-type supramolecular motif.

Bibliographic

Authors
Ren F, Li G, Zhang Q, Yao J, Zhang XQ
Journal
Acta Crystallogr Sect E Struct Rep Online
Year
2013 (2013-05-01)
PMID
23723884
DOI
10.1107/S1600536813009689
PMC
PMC3648264

Delivery context

The delivery route is not clearly identifiable from this paper. For hydrogen intake, inhalation is the most efficient route; inhalation, however, carries explosion risk (empirical LFL of 10%; high-concentration devices are not recommended).

Safety notes

The delivery route is not clearly identifiable from this paper. For hydrogen intake, inhalation is the most efficient route; inhalation, however, carries explosion risk (empirical LFL of 10%; high-concentration devices are not recommended).

See also:

Cite as: H2 Papers — PMID 23723884. https://h2-papers.org/en/papers/23723884
Source: PubMed PMID 23723884