2-fluorobenzaldehyde

CN(C)C(c1ccccc1F)c1c[nH]c2ccc(Cl)cc12
Reaction #9159
[(5-Chloro-1H-indol-3-yl)-(2-fluoro-phenyl)-methyl]-dimethyl-amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cc1ccc(-c2ccccc2F)n1-c1ccc(S(=O)(=O)N2CCCCC2)cc1
Reaction #46928
titled compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1ccc(-c2ccccc2F)n1-c1ccc(S(N)(=O)=O)cc1
Reaction #46929
titled compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1ccc(-c2ccccc2F)n1-c1ccc(S(=O)(=O)N2CCCCC2)cc1
Reaction #46930
titled compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Fc1ccccc1CNc1cc2c3c(c1)[C@@H]1CNCC[C@@H]1N3CCOC2
Reaction #51555
(7bR,11aS)-N-(2-fluorobenzyl)-1,2,7b,8,9,10,11,11a-octahydro-4H-[1,4]oxazepino[6,5,4-hi]pyrido[4,3-b]indol-6-amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
N#CC(C#N)=Cc1ccccc1F
Reaction #59443
title material
Rendimiento 28.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
O=C1CC(c2ccccc2F)Oc2ccc(O)cc21
Reaction #59485
2-(2-Fluorophenyl)-6-hydroxychroman-4-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
Fc1ccccc1CNC1CC1
Reaction #61318
Cyclopropyl-(2-fluorobenzyl)amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
Fc1ccccc1CNc1cc2c3c(c1)[C@@H]1CNCC[C@@H]1N3CCOC2
Reaction #75842
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CN1CCN=C(C=Cc2ccccc2Oc2ccc(Cl)cc2)c2ccc(F)cc21.Cl.Cl
Reaction #76610
(E)-5-[2-(4-chlorophenoxy)styryl]-8-fluoro-2,3-dihydro-1-methyl-1H-1,4-benzodiazepine dihydrochloride
Rendimiento 9.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CC(C)=CCC/C(C)=C/CC/C(C)=C/C=O
Reaction #76824
title compound
Rendimiento 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
O=C(O)CC1SC(c2ccccc2F)N(CCc2ccccc2)C1=O
Reaction #78916
2-[2-(2-Fluorophenyl)-3-(2-phenylethyl)-4-oxo-thiazolidin-5-yl]-acetic Acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
O=Cc1ccccc1Oc1ccc(I)cc1
Reaction #79761
2-(4-iodophenoxy) benzaldehyde
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
N#CC(=Cc1ccccc1F)C(O)C#N
Reaction #83634
2-Fluorobenzylidenemalonitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
COc1ccc(C2(O)C(c3ccccc3F)SC3=NCCCCN32)cc1OC.Cl
Reaction #95516
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
O=C(C=Cc1ccccc1F)C=Cc1ccccc1F
Reaction #164839
yellow crystals
Rendimiento 42.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
ON=Cc1ccccc1F
Reaction #170373
title compound
Rendimiento 97.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COc1cc(C=Cc2ccccc2F)cc(OC)c1C(C)C
Reaction #176179
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=Cc1ccccc1Sc1cccs1
Reaction #176980
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Fc1ccccc1CNc1cccc(-c2c(Cc3ccccc3)cnc3c(C(F)(F)F)cccc23)c1
Reaction #188667
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Página 1Siguiente