TY - JOUR
T1 - 8-Bromonaphthalen-1-amine
AU - Fuller, Amy L.
AU - Knight, Fergus R.
AU - Slawin, Alexandra M. Z.
AU - Woollins, J. Derek
PY - 2008/6
Y1 - 2008/6
N2 - The title compound, C10H8BrN, was obtained by slow addition of sodium azide to 8-bromo-1-naphthoic acid, followed by addition of aqueous ammonia. The crude product was crystallized from petroleum ether to give pink crystals. Compared to other 1,8-disubstituted naphthalene compounds, this compound exhibits less strain between the 1 and 8 substituents. Additionally, the NH protons form both intra- and intermolecular hydrogen bonds. The naphthalene units are arranged in a herring-bone stacking motif.
AB - The title compound, C10H8BrN, was obtained by slow addition of sodium azide to 8-bromo-1-naphthoic acid, followed by addition of aqueous ammonia. The crude product was crystallized from petroleum ether to give pink crystals. Compared to other 1,8-disubstituted naphthalene compounds, this compound exhibits less strain between the 1 and 8 substituents. Additionally, the NH protons form both intra- and intermolecular hydrogen bonds. The naphthalene units are arranged in a herring-bone stacking motif.
UR - http://www.scopus.com/inward/record.url?scp=57349196397&partnerID=8YFLogxK
U2 - 10.1107/S1600536808012580
DO - 10.1107/S1600536808012580
M3 - Article
SN - 1600-5368
VL - 64
JO - Acta Crystallographica. Section E, Structure reports online
JF - Acta Crystallographica. Section E, Structure reports online
ER -