1,3-dibromobenzene

CCCC(O)(C#Cc1cccc(Br)c1)CCC
Reaction #261059
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Brc1cccc(-c2cccnc2)c1
Reaction #262441
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
OC1(c2cccc(Br)c2)C2CCC1CN(Cc1ccccc1)C2
Reaction #265943
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC[Si](CC)(CC)c1cccc(Br)c1
Reaction #269502
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC1CC(O)(c2cccc(Br)c2)CCO1
Reaction #284923
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=[N+]([O-])c1ccc(Br)cc1Br
Reaction #285594
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCc1ccc(C(O)c2cccc(Br)c2)s1
Reaction #308222
3-bromophenyl-5-ethyl-2-thienylmethanol
Ausbeute 70.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
O=C(c1cccc(Br)c1)c1cc2ccc(F)cc2s1
Reaction #308251
3-bromophenyl 6-fluorobenzo[b]thiophen-2-yl ketone
Ausbeute 68.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
Clc1ccc(-c2cccc(Br)c2)cc1
Reaction #320776
3-(4-chlorophenyl)phenyl bromide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_01
Brc1cccc([Si](c2ccccc2)(c2ccccc2)c2ccc3c4ccccc4c4ccccc4c3c2)c1
Reaction #328683
(3-bromophenyl)diphenyl(triphenylen-2-yl)silane
Ausbeute 75.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
Brc1cccc(-c2ccccc2)c1
Reaction #335318
3-bromo biphenyl
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_05
CC12CC3(C)CC(c4cc(Br)cc(Br)c4)(C1)CC(C14CC5(C)CC(C)(CC(c6cc(Br)cc(Br)c6)(C5)C1)C4)(C2)C3
Reaction #338901
7,7′-bis(3,5-dibromophenyl)-3,3′,5,5′-tetramethyl-1,1′-biadamantane
Ausbeute 180.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
Brc1cccc(Oc2ccccc2)c1
Reaction #349021
1-bromo-3-phenoxybenzene
Ausbeute 38.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_05
C=C(c1ccc(SC)cc1)c1cccc(Br)c1
Reaction #382262
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
OC1(c2cccc(Br)c2)CCC1
Reaction #402557
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
C=C(c1cccc(Br)c1)c1ccc(OC(F)F)c(Cl)c1
Reaction #407737
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
Brc1cccc(Oc2ccccc2)c1
Reaction #409207
desired material
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_04
Brc1cccc(N2CCC2)c1
Reaction #418210
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
CN(c1cccc(Br)c1)C1CCCC1
Reaction #418219
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
O=C1CCCN1c1cccc(Br)c1
Reaction #418220
title compound
Ausbeute 67.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
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