2-bromo-1-(4-chlorophenyl)ethanone

O=C1NN=C(c2ccc(Cl)cc2)CS1
Reaction #1610
5-(4-chlorophenyl)-3H,6H-1,3,4-thiadiazin-2-one
Rendimiento 48.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C1NN=C(c2ccc(Cl)cc2)CS1
Reaction #1678
5-(4-chlorophenyl)-3H,6H-1,3,4-thiadiazin-2-one
Rendimiento 48.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C1NN=C(c2ccc(Cl)cc2)CS1
Reaction #2183
5-(4-chlorophenyl)-3H,6H-1,3,4-thiadiazin-2-one
Rendimiento 48.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C1NN=C(c2ccc(Cl)cc2)CS1
Reaction #2224
5-(4-chlorophenyl)-3H,6H-1,3,4-thiadiazin-2-one
Rendimiento 48.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C1NN=C(c2ccc(Cl)cc2)CS1
Reaction #2282
5-(4-chlorophenyl)-3H,6H-1,3,4-thiadiazin-2-one
Rendimiento 48.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C1NN=C(c2ccc(Cl)cc2)CS1
Reaction #72560
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=C(CO)c1ccc(Cl)cc1
Reaction #72564
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CS(=O)(=O)c1ccc(-n2cc(-c3ccc(Cl)cc3)nc2-c2ccc(Cl)cc2)cc1
Reaction #80582
2,4-bis-(4-chlorophenyl)-1-[4-(methylsulfonyl)phenyl]-1H-imidazole
Rendimiento 55.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
Nc1[nH]c2c(CC(=O)c3ccc(Cl)cc3)cccc2[n+]1CCN1CCOCC1.[Br-]
Reaction #82979
title compound
Rendimiento 95.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
O=C1CC(c2ccc(Cl)cc2)CO1
Reaction #93537
title compound
Rendimiento 71.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_09
O=C(CN1CCC(N2Cc3ccccc3NC2=O)CC1)c1ccc(Cl)cc1
Reaction #95354
desired product
Rendimiento 56.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
[Br-]
Reaction #181696
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(c1ccc(Cl)cc1)C(O)O
Reaction #189938
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)CCNc1nonc1-c1nc2ccccc2n1CC(=O)c1ccc(Cl)cc1
Reaction #198301
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
N#CCCNc1nonc1-c1nc2ccccc2n1CC(=O)c1ccc(Cl)cc1
Reaction #219183
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
COC(=O)CCNc1nonc1-c1nc2ccccc2n1CC(=O)c1ccc(Cl)cc1
Reaction #219187
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
O=C(Cn1c(-c2nonc2NCCCO)nc2ccccc21)c1ccc(Cl)cc1
Reaction #219189
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
Cn1c(N2CCN(CC(=O)c3ccc(Cl)cc3)CC2)cc(=O)n(C)c1=O
Reaction #226034
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CON=C(CBr)c1ccc(Cl)cc1
Reaction #229753
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(CN1CCNC(=O)C1c1ccccc1)c1ccc(Cl)cc1
Reaction #265850
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
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