Peer-reviewedCC BYIUCrData
6,7-Di-bromo-2-methyl-3-phenyl-quinoxaline.
- 1Department of Chemistry & Biochemistry Central Connecticut State University, 1619 Stanley Street New Britain CT 06053 USA.
- 2The University of Edinburgh School of Chemistry Joseph Black Building David Brewster Road Edinburgh EH9 3FJ United Kingdom.
Abstract
The title com-pound, C15H10Br2N2, was synthesized using the acid catalyst NH4HF2 in a water/methanol solution. There are two mol-ecules per asymmetric unit where the quinoxaline moieties make dihedral angles of 48.05 (4) and 40.83 (5)° with respect to their phenyl rings. In the extended structure, mol-ecules form layers stacked along (001) that are held together by hy-dro-gen and halogen bonds.
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BibTeX
@article{valentin202667dibromo2methyl3phenylquinoxaline,
title = {{6,7-Di-bromo-2-methyl-3-phenyl-quinoxaline.}},
author = {Avion T Valentin and Guy Crundwell and Gary S Nichol},
journal = {IUCrData},
year = {2026},
month = sep,
doi = {10.1107/s2414314626010278},
url = {https://europepmc.org/article/MED/42997249},
note = {CC BY},
}
RIS
TY - JOUR
TI - 6,7-Di-bromo-2-methyl-3-phenyl-quinoxaline.
AU - Avion T Valentin
AU - Guy Crundwell
AU - Gary S Nichol
PY - 2026
DA - 2026/09/01
JO - IUCrData
DO - 10.1107/s2414314626010278
UR - https://europepmc.org/article/MED/42997249
AB - The title com-pound, C15H10Br2N2, was synthesized using the acid catalyst NH4HF2 in a water/methanol solution. There are two mol-ecules per asymmetric unit where the quinoxaline moieties make dihedral angles of 48.05 (4) and 40.83 (5)° with respect to their phenyl rings. In the extended structure, mol-ecules form layers stacked along (001) that are held together by hy-dro-gen and halogen bonds.
SN - 2414-3146
ER -