2-chloro-1-(4-fluorophenyl)ethanone

CON=C(CBr)c1ccc(F)cc1
Reaction #61627
2-bromo-1-(4-fluorophenyl)ethanone O-methyloxime
Yield 83.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CC(=O)N1CCN(CC(=O)c2ccc(F)cc2)CC1.Cl
Reaction #78074
1-acetyl-4-(4-fluorophenylcarbonylmethyl)-piperazine hydrochloride
Yield 99.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CS(=O)(=O)c1ccc(-n2cc(-c3ccc(F)cc3)nc2-c2ccc(Cl)cc2)cc1
Reaction #80579
2-(4-chlorophenyl) -4-(4-fluorophenyl)-1-[4-(methylsulfonyl)phenyl]-1H-imidazole
Yield 36.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CCOC(=O)N1CCN(CC(=O)c2ccc(F)cc2)CC1
Reaction #211766
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)N1CC2CC(CN(CC(=O)c3ccc(F)cc3)C2)C1
Reaction #216725
amine
Yield 86.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11
Fc1ccc(C2CO2)cc1
Reaction #222049
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)N1CC2CC(CN(CC(=O)c3ccc(F)cc3)C2)C1
Reaction #271041
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COc1ccc2c(c1)C(N1CCN(CC(=O)c3ccc(F)cc3)CC1)CC2
Reaction #391284
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CC(=O)Nc1ccc(C(=O)C2CCN(CC(=O)c3ccc(F)cc3)CC2)cc1
Reaction #393171
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
O=C(Cn1cc[n+](CC(OCc2ccc(Cl)cc2Cl)c2ccc(Cl)cc2Cl)c1)c1ccc(F)cc1.[Cl-]
Reaction #415821
1-[2,4-dichloroβ-(2,4-dichlorobenzyloxy)phenethyl]-3-(p-fluorobenzoylmethyl)imidazolium chloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1977_04
CS(=O)(=O)CC(=O)c1ccc(F)cc1
Reaction #422617
1-(4-fluorophenyl)-2-methylsulfonylethan-1-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
C=CCN(CC=C)CC(=O)c1ccc(F)cc1
Reaction #425256
crude title compound
Yield 118.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
C#CCC1(c2ccc(F)cc2)CO1
Reaction #501823
4,5-epoxy-4-(4'-fluorophenyl)-1-pentyne
Yield 79.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_12
C#CC1(c2ccc(F)cc2)CO1
Reaction #501827
3,4-epoxy- 3-(4'-fluorophenyl)-1-butyne
Yield 66.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_12
CC(=O)OCC(=O)c1ccc(F)cc1
Reaction #554636
compound
Yield 78.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_01
C=CCN(CC=C)CC(=O)c1ccc(F)cc1
Reaction #557384
crude title compound
Yield 118.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_01
CC(=O)Nc1ccc(C(=O)C2CCN(CC(=O)c3ccc(F)cc3)CC2)cc1
Reaction #573778
1-(4-Fluorophenyl)-2-[4-[(4-acetamidophenyl)carbonyl]-1-piperidinyl]-ethanone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1994_03
CCOC(=O)N1CCN(CC(=O)c2ccc(F)cc2)CC1
Reaction #584502
1-ethoxycarbonyl-4-[2-(4-fluorophenyl)-2-oxoethyl]piperazine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_09
Fc1ccc(C2CO2)cc1
Reaction #584534
2-(4-fluorophenyl)oxirane
Yield 106.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_09
CS(=O)(=O)CC(=O)c1ccc(F)cc1
Reaction #666431
1-(4-fluorophenyl)-2-methylsulfonylethan-1-one
Yield 86.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_05
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