4-Bromobenzaldehyde

Brc1ccc(C2OCCO2)cc1
Reaction #6702
2-(4-bromophenyl)-1,3-dioxolane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Brc1ccc(C=Cc2ccc(Br)cc2)cc1
Reaction #7291
desired product
Yield 65.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COc1ccccc1-c1ccc(C=O)cc1
Reaction #9072
title compound
Yield 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=Cc1ccc(-c2cccs2)cc1
Reaction #9074
title compound
Yield 78.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=Cc1ccc(-c2nccs2)cc1
Reaction #10718
4-Thiazol-2-yl-benzaldehyde
Yield 82.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
C[Si](C)(C)C#Cc1ccc(C=O)cc1
Reaction #42158
4-[(trimethylsilyl)ethynyl]benzaldehyde
Yield 88.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
C[Si](C)(C)C#Cc1ccc(C=O)cc1
Reaction #42177
4-[(trimethylsilyl)ethynyl]benzaldehyde
Yield 88.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCCCC(O)c1ccc(Br)cc1
Reaction #43280
4
Yield 76.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COC(=O)c1ccc(NCc2ccc(Br)cc2)cc1O
Reaction #46719
yellow solid
Yield 58.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1ccc(-c2ccc(Br)cc2)n1-c1ccc(S(N)(=O)=O)cc1
Reaction #46926
titled compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(C)OC(=O)Nc1ccc(Cl)cc1C(O)c1ccc(Br)cc1
Reaction #47968
tert-butyl {2-[(4-bromophenyl)(hydroxy)methyl]-4-chlorophenyl}carbamate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
N#CC=Cc1ccc(Br)cc1
Reaction #51198
3-(4-Bromophenyl)-2-propenenitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
[O-][N+](=Cc1ccc(Br)cc1)c1ccc(Cl)cc1
Reaction #56195
α-p-bromophenyl-N-p-chlorophenylnitrone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
Cc1ccc(S(=O)(=O)C(NC=O)c2ccc(Br)cc2)cc1
Reaction #60855
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CC(C)C(N=Cc1ccc(Br)cc1)C(C)C
Reaction #64307
(4-bromobenzylidene)(1-isopropyl-2-methylpropyl)amine
Yield 94.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
COC(OC)c1ccc(Br)cc1
Reaction #64308
1-bromo-4-(dimethoxymethyl)benzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
C[C@H]1CN(Cc2ccc(Br)cc2)CCN1C(=O)OCc1ccccc1
Reaction #71618
title compound
Yield 84.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=C(OCc1ccccc1)N1CCN(Cc2ccc(Br)cc2)CC1
Reaction #71628
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
C[C@@H]1CN(Cc2ccc(Br)cc2)C[C@H](C)N1C(=O)OC(C)(C)C
Reaction #71631
title compound
Yield 91.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
OC(c1ccc(Cl)cc1)c1ccc(Br)cc1
Reaction #73801
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
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