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1163436

CC(=O)Nc1c([N+](=O)[O-])cc(Br)cc1C(F)(F)F
Reaction #82048
2-acetamido-5-bromo-3-nitrobenzotrifluoride
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1c([N+](=O)[O-])cc(Br)cc1C(F)(F)F
Reaction #82049
2-amino-5-bromo-3-nitrobenzotrifluoride
Ausbeute 75.6%DOI: 10.6084/m9.figshare.5104873.v1
Nc1cc(Br)cc(C(F)(F)F)c1N
Reaction #82050
2,3-diamino-5-bromobenzotrifluoride
Ausbeute 64.6%DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]c2cc(Br)cc(C(F)(F)F)c2[nH]c1=O
Reaction #82051
title compound
Ausbeute 71.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1c([N+](=O)[O-])cc(Br)cc1C(F)(F)F
Reaction #82636
2-acetamido-5-bromo-3-nitrobenzotrifluoride
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1c([N+](=O)[O-])cc(Br)cc1C(F)(F)F
Reaction #82637
2-amino-5-bromo-3-nitrobenzotrifluoride
Ausbeute 75.6%DOI: 10.6084/m9.figshare.5104873.v1
Nc1cc(Br)cc(C(F)(F)F)c1N
Reaction #82638
2,3-diamino-5-bromobenzotrifluoride
Ausbeute 64.6%DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]c2cc(Br)cc(C(F)(F)F)c2[nH]c1=O
Reaction #82639
title compound
Ausbeute 71.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)N(Cc1cccc(C(F)(F)F)c1)c1c(N)cc(Br)cc1C(F)(F)F
Reaction #187124
DOI: 10.1039/C8SC04228D
CCOC(=O)N(Cc1ccc(OC)cc1OC)c1c([N+](=O)[O-])cc(Br)cc1C(F)(F)F
Reaction #281083
DOI: 10.1039/C8SC04228D
CC(=O)Nc1c([N+](=O)[O-])cc(Br)cc1C(F)(F)F
Reaction #526670
2-acetamido-5-bromo-3-nitrobenzotrifluoride
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1c([N+](=O)[O-])cc(Br)cc1C(F)(F)F
Reaction #526671
2-amino-5-bromo-3-nitrobenzotrifluoride
Ausbeute 75.6%DOI: 10.6084/m9.figshare.5104873.v1
Nc1cc(Br)cc(C(F)(F)F)c1N
Reaction #526672
2,3-diamino-5-bromobenzotrifluoride
Ausbeute 64.6%DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]c2cc(Br)cc(C(F)(F)F)c2[nH]c1=O
Reaction #526673
title compound
Ausbeute 71.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)Nc1c([N+](=O)[O-])cc(Br)cc1C(F)(F)F
Reaction #582812
title compound
Ausbeute 61.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)N(Cc1ccccc1Cl)c1c([N+](=O)[O-])cc(Br)cc1C(F)(F)F
Reaction #582813
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)N(Cc1ccccc1Cl)c1c([N+](=O)[O-])cc(C#N)cc1C(F)(F)F
Reaction #582814
title compound
Ausbeute 59.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)N(Cc1cccc(C(F)(F)F)c1)c1c([N+](=O)[O-])cc(Br)cc1C(F)(F)F
Reaction #582835
title compound
Ausbeute 82.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)N(Cc1cccc(C(F)(F)F)c1)c1c(N)cc(Br)cc1C(F)(F)F
Reaction #582836
title compound
Ausbeute 100.4%DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]c2cc(Br)cc(C(F)(F)F)c2n1Cc1cccc(C(F)(F)F)c1
Reaction #582837
title compound
Ausbeute 106.2%DOI: 10.6084/m9.figshare.5104873.v1
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