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Ethyl 3,7-dichloro­quinoline-8-carboxyl­ate

TLDR
The title compound, C12H9Cl2NO2, was prepared by the esterification of 3,7-dichloroquinoline-8-carboxylic acid with triethyl phosphite by stabilized by aromatic π–π stacking between the benzene and the pyridine rings of neighbouring molecules.
Abstract
The title compound, C12H9Cl2NO2, was prepared by the esterification of 3,7-dichloro­quinoline-8-carboxylic acid with triethyl phosphite. The crystal structure is stabilized by aromatic π–π stacking between the benzene and the pyridine rings of neighbouring mol­ecules [centroid–centroid distances = 3.716 (2) and 3.642 (2) A]. In addition, weak inter­molecular C—H⋯N hydrogen bonds are present in the structure.

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Journal ArticleDOI

A short history of SHELX

TL;DR: This paper could serve as a general literature citation when one or more of the open-source SH ELX programs (and the Bruker AXS version SHELXTL) are employed in the course of a crystal-structure determination.
Journal ArticleDOI

ORTEP-3 for Windows - a version of ORTEP-III with a Graphical User Interface (GUI)

TL;DR: L Lists of software presented and~or reviewed in the Journal of Applied Crystallography are available on the World Wide Web at the above address, together with information about the availability of the software where this is known.
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Single-crystal structure validation with the program PLATON

TL;DR: The results of a single-crystal structure determination when in CIF format can now be validated routinely by automatic procedures, and the concepts of validation and the classes of checks carried out by the program PLATON as part of the IUCr checkCIF facility are described.
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Oxidative injury induced by the herbicide quinclorac on Echinochloa oryzicola Vasing. and the involvement of antioxidative ability in its highly selective action in grass species

TL;DR: The results suggest that the difference in hereditary antioxidative ability is one factor that results in the particularly high selectivity of quinclorac between rice and E. oryzicola.
Journal ArticleDOI

Resistance of barnyardgrass (Echinochloa crus‐galli) to atrazine and quinclorac

TL;DR: Chlorophyll fluorescence and Hill reaction analysis supported the view that the mechanism of resistance to atrazine in the X biotype was modification of the target site, the DI protein, and quinclorac is not a PS II inhibiting herbicide.
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