6-bromo-2-naphthoic acid

O=C(Cl)c1ccc2cc(Br)ccc2c1
Reaction #84030
6-bromo-2-naphthoyl chloride
收率 100.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
O=C(Cl)c1ccc2cc(Br)ccc2c1
Reaction #159011
6-bromonaphthalene-2-carbonyl chloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C(O)c1ccc2cc(C3(O)CCn4cncc43)ccc2c1
Reaction #159258
title compound
收率 12.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C(Cl)c1ccc2cc(Br)ccc2c1
Reaction #166962
6-bromonaphthalene-2-carbonyl chloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C(Nc1ccc2c(c1)OCCO2)c1ccc2cc(Br)ccc2c1
Reaction #239553
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
NC(=O)c1ccc2cc(Br)ccc2c1
Reaction #254797
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(Cl)c1ccc2cc(Br)ccc2c1
Reaction #282181
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCOC(=O)c1ccc2cc(Br)ccc2c1
Reaction #411407
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_04
NC(=O)c1ccc2cc(Br)ccc2c1
Reaction #478516
title compound
收率 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
O=C(Cl)c1ccc2cc(Br)ccc2c1
Reaction #504713
6-bromonaphthalene-2-carbonyl chloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
CNC(=O)c1ccc2cc(Br)ccc2c1
Reaction #507394
6-bromo-N-methyl-2-naphthamide
收率 80.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
CCOC(=O)c1ccc2cc(Br)ccc2c1
Reaction #583119
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_09
CCOC(=O)c1ccc2cc(Br)ccc2c1
Reaction #700510
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_12
CCOC(=O)c1ccc2cc(Br)ccc2c1
Reaction #705239
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_09
CCOC(=O)c1ccc2cc(Br)ccc2c1
Reaction #706767
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_09
NC(=O)c1ccc2cc(Br)ccc2c1
Reaction #757959
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
CCOC(=O)c1ccc2cc(Br)ccc2c1
Reaction #771164
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
CNC(=O)c1ccc2cc(Br)ccc2c1
Reaction #811384
title compound
收率 95.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_11
O=C(NC1CC1)c1ccc2cc(Br)ccc2c1
Reaction #811385
title compound
收率 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_11
O=C(NC1CCC1)c1ccc2cc(Br)ccc2c1
Reaction #811386
title compound
收率 72.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_11
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