6-bromo-2-naphthoyl chloride

CON(C)C(=O)c1ccc2cc(Br)ccc2c1
Reaction #84031
6-bromo-N-methoxy-N-methyl-2-naphthamide
Выход 100.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
[N-]=[N+]=CC(=O)c1ccc2cc(Br)ccc2c1
Reaction #159012
1-(6-bromonaphthalen-2-yl)-2-diazoethanone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
[N-]=[N+]=CC(=O)c1ccc2cc(Br)ccc2c1
Reaction #166963
1-(6-bromonaphthalen-2-yl)-2-diazoethanone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C(Nc1cnc2ccccc2c1)c1ccc2cc(Br)ccc2c1
Reaction #228472
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(=O)Nc1nc2c(NC(=O)c3ccc4cc(Br)ccc4c3)cccc2s1
Reaction #279739
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
[N-]=[N+]=CC(=O)c1ccc2cc(Br)ccc2c1
Reaction #397239
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
[N-]=[N+]=CC(=O)c1ccc2cc(Br)ccc2c1
Reaction #504714
1-(6-bromonaphthalen-2-yl)-2-diazoethanone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
Nc1nc2c(NC(=O)c3ccc4cc(Br)ccc4c3)cccc2s1
Reaction #780554
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
CC(C)N(C(=O)c1ccc2cc(Br)ccc2c1)C(C)C
Reaction #1149061
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_11
O=C(Nc1ccc2[nH]cnc2c1)c1ccc2cc(Br)ccc2c1
Reaction #1200058
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
[N-]=[N+]=CC(=O)c1ccc2cc(Br)ccc2c1
Reaction #1272931
1-(6-bromonaphthalen-2-yl)-2-diazoethanone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_03
CON(C)C(=O)c1ccc2cc(Br)ccc2c1
Reaction #1573580
6-bromo-N-methoxy-N-methyl-2-naphthamide
Выход 100.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_08
O=C(Nc1ccc2c(c1)NCC(CO)C2)c1ccc2cc(Br)ccc2c1
Reaction #2072153
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_06
Nc1nc2c(NC(=O)c3ccc4cc(Br)ccc4c3)cccc2s1
Reaction #2074996
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_06
CC(=O)Nc1nc2c(NC(=O)c3ccc4cc(Br)ccc4c3)cccc2s1
Reaction #2074997
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_06
O=C(Nc1ccc2[nH]cnc2c1)c1ccc2cc(Br)ccc2c1
Reaction #2074998
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_06
O=C(Nc1cnc2ccccc2c1)c1ccc2cc(Br)ccc2c1
Reaction #2074999
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_06
[N-]=[N+]=CC(=O)c1ccc2cc(Br)ccc2c1
Reaction #2126256
1-(6-bromonaphthalen-2-yl)-2-diazoethanone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_11
O=C(Nc1ccc2c(c1)NCC(CO)C2)c1ccc2cc(Br)ccc2c1
Reaction #2414510
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (10/10)
CC(C)N(C(=O)c1ccc2cc(Br)ccc2c1)C(C)C
Reaction #2432939
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (10/10)