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Acta Crystallographica Section E
Article . 2009 . Peer-reviewed
License: CC BY
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Acta Crystallographica Section E
Article
License: CC BY
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Other literature type . 2009
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Acta Crystallographica Section E
Article . 2009
Data sources: DOAJ
https://dx.doi.org/10.60692/vv...
Other literature type . 2009
Data sources: Datacite
https://dx.doi.org/10.60692/5d...
Other literature type . 2009
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5,7-Dichloroquinolin-8-ol

5,7 -ديكلوروكينولين-8 -أول
Authors: Seik Weng Ng;

5,7-Dichloroquinolin-8-ol

Abstract

The mol­ecule of the title compound, C9H5Cl2NO, is essentially planar [give maximum or r.m.s. deviation] and the hydr ­oxy group acts as a hydrogen-bond donor to the N atom of a symmetry-related mol­ ecule, generating a hydrogen-bonded dimer,which lies on a twofold rotation axis.

The mol­ecule of the title compound, C9H5Cl2NO, is essentially planar [give maximum or r.m.s. deviation] and the hydr­oxy group acts as a hydrogen-bond donor to the N atom of a symmetry-related mol­ecule, generating a hydrogen-bonded dimer,which lies on a twofold rotation axis.

The mol­ecule of the title compound, C9H5Cl2NO, is essentially planar [give maximum or r.m.s. deviation] and the hydr­oxy group acts as a hydrogen-bond donor to the N atom of a symmetry-related mol­ecule, generating a hydrogen-bonded dimer,which lies on a twofold rotation axis.

The molecule ofthe title compound, C9H5Cl2NO, is essentially planar [give maximum or r.m.s. deviation] and the hydr-oxy group acts as a hydrogen-bond donor to the N atom of a symmetry-related molecule, generating a hydrogen-bonded dimer,which lies on a twofold rotation axis.

يكون جزيء مركب العنوان، C9H5Cl2NO، مستويًا بشكل أساسي [يعطي أقصى انحراف أو انحراف RMS] وتعمل مجموعة hydr - oxy كمانح لرابطة الهيدروجين لذرة N لجزيء مرتبط بالتماثل، مما يولد دايمرًا مرتبطًا بالهيدروجين،والذي يقع على محور دوران مزدوج.

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Keywords

Parallel computing, Symmetry (geometry), Geometry, Organic chemistry, Organic Papers, Inorganic Chemistry, FOS: Chemical sciences, FOS: Mathematics, Atom (system on chip), Asymmetric Catalysis, Hydrogen bond, Indolizine Synthesis and Bioactivity Studies, Crystallography, Group (periodic table), Computer graphics (images), Organic Chemistry, Molecule, Hydrogen Bonding, Computer science, Chemical Crystallography, Chemistry, Dimer, QD901-999, Physical Sciences, Planar, Rotation (mathematics), Mathematics, Hydrogen

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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
1
Average
Average
Average
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gold