4-Iodobenzotrifluoride

CC(C)(C)OC(=O)N1CCC(c2ccccc2Sc2ccc(C(F)(F)F)cc2)CC1
Reaction #43516
4-[2-(4-trifluoromethyl-phenylsulfanyl)-phenyl]-piperidine-1-carboxylic acid tert-butyl ester
Выход 59.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COC(=O)[C@H](Cc1ccc(C(F)(F)F)cc1)C(=O)OC(C)(C)C
Reaction #48300
(S)-methyl 2-(tert-butoxycarbonyl)-3-(4-(trifluoromethyl)phenyl)propanoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1c(C#Cc2ccc(C(F)(F)F)cc2)ccc(N)c1C#N
Reaction #80918
2-amino-6-methyl-5-[(4-trifluoromethylphenyl)ethynyl]benzonitrile
Выход 72.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
FC(F)(F)c1ccc(-n2cnc(Br)n2)cc1
Reaction #90311
title compound
Выход 64.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
N#Cc1nc(C#Cc2ccc(C(F)(F)F)cc2)cnc1N
Reaction #178760
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)C(=O)Nc1cccc(C2CCN(Cc3ccc4c(ccn4-c4ccc(C(F)(F)F)cc4)c3)CC2)c1
Reaction #184066
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)C1(c2ccc(-c3ccc(-c4onc(C)c4C(O)CC=Cc4ccc(C(F)(F)F)cc4)cc3)cc2)CC1
Reaction #235154
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1noc(C)c1S(=O)(=O)N1CCC2(CCN(c3ccc(C(F)(F)F)cc3)C2=O)CC1
Reaction #247158
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
FC(F)(F)c1ccc(-n2ccc3ccc(Cl)cc32)cc1
Reaction #257240
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1c(C#Cc2ccc(C(F)(F)F)cc2)cnc(N)c1C#N
Reaction #320792
2-amino-3-cyano-4-methyl-5-[(4-trifluoromethylphenyl)ethynyl]pyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_01
Cn1nccc1-c1ccc(C(F)(F)F)cc1
Reaction #325536
title compound
Выход 110.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
Cn1nccc1-c1cnn(-c2ccc(C(F)(F)F)cc2)c1
Reaction #325553
title compound
Выход 80.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
O=c1cc(-c2ccc(C(F)(F)F)cc2)cc(C(F)(F)F)o1
Reaction #356219
solid
Выход 100.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_11
Cc1c(C#Cc2ccc(C(F)(F)F)cc2)ccc(N)c1C#N
Reaction #450956
2-amino-6-methyl-5-[(4-trifluoromethylphenyl)ethynyl]benzonitrile
Выход 72.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_02
O=C1CSCCN1c1ccc(C(F)(F)F)cc1
Reaction #499170
title product
Выход 23.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_05
CCO[PH](=O)c1ccc(C(F)(F)F)cc1
Reaction #507280
ethyl 4-(trifluoromethyl)phenylphosphinate
Выход 28.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
N#Cc1nc(C#Cc2ccc(C(F)(F)F)cc2)cnc1N
Reaction #528084
2-amino-3-cyano-5-[(4-trifluoromethylphenyl)ethynyl]pyrazine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_05
CCO[PH](=O)c1ccc(C(F)(F)F)cc1
Reaction #536015
ethyl 4-(trifluoromethyl)phenylphosphinate
Выход 28.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
O=Cc1ccccc1-c1ccc(C(F)(F)F)cc1
Reaction #570467
oil
Выход 136.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_03
CCO[PH](=O)c1ccc(C(F)(F)F)cc1
Reaction #604192
ethyl 4-(trifluoromethyl)phenylphosphinate
Выход 28.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_08
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