2-Bromo-2-methyl-N-(4-nitrophenyl)propanamide

Rodolfo Moreno-Fuquen; David E. Quintero; Fabio Zuluaga; Roberto L. A. Haiduke; Alan R. Kennedy

doi:10.1107/S1600536811005320

2-Bromo-2-methyl-N-(4-nitrophenyl)propanamide

Rodolfo Moreno-Fuquen, David E. Quintero, Fabio Zuluaga, Roberto L. A. Haiduke, Alan R. Kennedy

Pure And Applied Chemistry

Research output: Contribution to journal › Article › peer-review

5 Citations (Scopus)

Abstract

The title compound, C10H11BrN2O3, exhibits a small twist between the amide residue and benzene ring [the C-N-C-C torsion angle = 12.7 (4)degrees]. The crystal structure is stabilized by weak N-H center dot center dot center dot O, C-H center dot center dot center dot Br and C-H center dot center dot center dot O interactions. These lead to supramolecular layers in the bc plane.

Original language	English
Article number	O659
Number of pages	10
Journal	Acta Crystallographica Section E: Structure Reports
Volume	67
Issue number	3
DOIs	https://doi.org/10.1107/S1600536811005320
Publication status	Published - Mar 2011

Keywords

hydrogen-bond patterns
crystals

Access to Document

10.1107/S1600536811005320Licence: CC BY 4.0

Link to publication in Scopus

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1 Finished

Physical Organic Chemistry: Opportunities In Synthesis, Materials And Pharmaceuticals (Science And Innovation Award)
Murphy, J., Coombs, G., Ferguson, A. & Florence, A.
Scottish Funding Council SFC, EPSRC (Engineering and Physical Sciences Research Council)
1/09/07 → 30/10/12
Project: Research

x-ray diffractometer
Alan Kennedy (Manager)
Pure And Applied Chemistry
Facility/equipment: Equipment

Cite this

@article{48fa953e204443c08ecb633aa80513bd,

title = "2-Bromo-2-methyl-N-(4-nitrophenyl)propanamide",

abstract = "The title compound, C10H11BrN2O3, exhibits a small twist between the amide residue and benzene ring [the C-N-C-C torsion angle = 12.7 (4)degrees]. The crystal structure is stabilized by weak N-H center dot center dot center dot O, C-H center dot center dot center dot Br and C-H center dot center dot center dot O interactions. These lead to supramolecular layers in the bc plane.",

keywords = "hydrogen-bond patterns, crystals",

author = "Rodolfo Moreno-Fuquen and Quintero, {David E.} and Fabio Zuluaga and Haiduke, {Roberto L. A.} and Kennedy, {Alan R.}",

year = "2011",

month = mar,

doi = "10.1107/S1600536811005320",

language = "English",

volume = "67",

journal = "Acta Crystallographica Section E: Structure Reports",

issn = "1600-5368",

number = "3",

}

TY - JOUR

T1 - 2-Bromo-2-methyl-N-(4-nitrophenyl)propanamide

AU - Moreno-Fuquen, Rodolfo

AU - Quintero, David E.

AU - Zuluaga, Fabio

AU - Haiduke, Roberto L. A.

AU - Kennedy, Alan R.

PY - 2011/3

Y1 - 2011/3

N2 - The title compound, C10H11BrN2O3, exhibits a small twist between the amide residue and benzene ring [the C-N-C-C torsion angle = 12.7 (4)degrees]. The crystal structure is stabilized by weak N-H center dot center dot center dot O, C-H center dot center dot center dot Br and C-H center dot center dot center dot O interactions. These lead to supramolecular layers in the bc plane.

AB - The title compound, C10H11BrN2O3, exhibits a small twist between the amide residue and benzene ring [the C-N-C-C torsion angle = 12.7 (4)degrees]. The crystal structure is stabilized by weak N-H center dot center dot center dot O, C-H center dot center dot center dot Br and C-H center dot center dot center dot O interactions. These lead to supramolecular layers in the bc plane.

KW - hydrogen-bond patterns

KW - crystals

UR - http://www.scopus.com/inward/record.url?scp=79952393637&partnerID=8YFLogxK

U2 - 10.1107/S1600536811005320

DO - 10.1107/S1600536811005320

M3 - Article

VL - 67

JO - Acta Crystallographica Section E: Structure Reports

JF - Acta Crystallographica Section E: Structure Reports

SN - 1600-5368

IS - 3

M1 - O659

ER -

2-Bromo-2-methyl-N-(4-nitrophenyl)propanamide

Abstract

Keywords

Access to Document

Physical Organic Chemistry: Opportunities In Synthesis, Materials And Pharmaceuticals (Science And Innovation Award)

x-ray diffractometer

Cite this