1-(4-Methylbenzenesulfonyl)-1-phenyl-1 <i>H</i> ,2 <i>H</i> -cyclobuta[ <i>c</i> ]quinoline

The title compound, C<sub>24</sub>H<sub>19</sub>NO<sub>2</sub>S, forms strands along the <i>b</i>-axis direction <i>via</i> hydrogen bonds from the tolyl group to the sulfonyl oxygen atoms. The tricyclic framework is almost planar and the two six-membered aromatic substituents are nearly coparallel.

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Publication Details

Journal
IUCrData
Published
2025-11-13
DOI
https://doi.org/10.1107/s2414314625010193
Citations
1
Primary Topic
Crystal structures of chemical compounds
Type
article
Field-Weighted Citation Impact
0.54
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article

1-(4-Methylbenzenesulfonyl)-1-phenyl-1 H ,2 H -cyclobuta[ c ]quinoline

Benjamin Dassonneville, Heiner Detert, Dieter Schollmeyer
1 citations
IUCrData
Crystal structures of chemical compounds
0.54
article

1-(4-Methylbenzenesulfonyl)-1-phenyl-1 H ,2 H -cyclobuta[ c ]quinoline

Benjamin Dassonneville, Heiner Detert, Dieter Schollmeyer
article en
1 citations

Abstract

The title compound, C<sub>24</sub>H<sub>19</sub>NO<sub>2</sub>S, forms strands along the <i>b</i>-axis direction <i>via</i> hydrogen bonds from the tolyl group to the sulfonyl oxygen atoms. The tricyclic framework is almost planar and the two six-membered aromatic substituents are nearly coparallel.

IUCrDataVol. 10(11)
Johannes Gutenberg University Mainz (DE)
Openalex Percentile: Top 28%
Crystal structures of chemical compounds
0.54
DOIOpen Access PDFOpenAlex
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1-(4-Methylbenzenesulfonyl)-1-phenyl-1 <i>H</i> ,2 <i>H</i> -cyclobuta[ <i>c</i> ]quinoline — Benjamin Dassonneville, Heiner Detert, et al. · IUCrData (2025) | TGRS Research Map | TGRS