Abstract

In the title compound, C(11)H(14)N(2)O(5)S, the amide O atom acts as a hydrogen-bond acceptor from a carboxyl-ate O atom and a secondary amino N atom. In addition, one of the sulfonyl O atoms and the carbonyl O atom of the carboxyl group also form hydrogen bonds with the primary amido N atom. These intermolecular hydrogen-bonding inter-actions give rise to a layer structure, with the layers parallel to the ac plane.

Keywords:
Amide Intermolecular force Sulfonyl Atom (system on chip) Hydrogen bond Acceptor Group (periodic table)

Metrics

0
Cited By
0.00
FWCI (Field Weighted Citation Impact)
0
Refs
0.46
Citation Normalized Percentile
Is in top 1%
Is in top 10%

Topics

Crystal structures of chemical compounds
Physical Sciences →  Chemistry →  Inorganic Chemistry
Crystallography and molecular interactions
Physical Sciences →  Chemistry →  Physical and Theoretical Chemistry
Nonlinear Optical Materials Research
Physical Sciences →  Materials Science →  Electronic, Optical and Magnetic Materials

Related Documents

JOURNAL ARTICLE

N-(p-Tolylsulfonyl)-L-asparagine

Muhammad Nadeem ArshadH. Mubashar-Ur-RehmanIslam Ullah KhanMuhammad ShafiqKong Mun Lo

Journal:   Acta Crystallographica Section E Structure Reports Online Year: 2010 Vol: 66 (3)Pages: o541-o541
JOURNAL ARTICLE

Oxidation of N-(p-tolylsulfonyl)sulfilimines to N-(p-tolylsulfonyl)sulfoximines with alkaline hydrogen peroxide

Carl R. JohnsonRobert Kirchhoff

Journal:   The Journal of Organic Chemistry Year: 1979 Vol: 44 (13)Pages: 2280-2280
JOURNAL ARTICLE

Coordination properties of N-p-tolylsulfonyl-l-glutamic acid toward metalII

Marco BorsariLedi MenabueMonica Saladini

Journal:   Polyhedron Year: 1999 Vol: 18 (14)Pages: 1983-1989
© 2026 ScienceGate Book Chapters — All rights reserved.