di(propan-2-yl)azanide

O=[N+]([O-])c1ccccc1OC(CCl)CCl
Reaction #61384
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CCCCC1CCc2cc(OC)ccc2C1=O
Reaction #173041
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)OC(=O)Nc1ccc(F)c(C=O)c1F
Reaction #173635
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCC(C(=O)O)C(C)(C)c1ccccc1
Reaction #173646
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc(Br)cc1CCc1sccc1C(=O)O
Reaction #174395
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1cc(Nc2nccc(C(F)(F)F)n2)cc(-c2cnc(C=O)s2)c1
Reaction #174490
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc(Cl)cc1C(=O)C=C1SC(C(C)(C)O)=C(C)N1CC1CCC1
Reaction #174709
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)CC1(C(CO)C(=O)OC(C)(C)C)CCN(CCc2ccccc2)C1=O
Reaction #174789
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=S(=O)(c1ccccc1)n1c(C(O)CC2CCCO2)cc2cccnc21
Reaction #174826
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC1COCCN1c1nc(Cl)nc2c1nc(I)n2C
Reaction #175862
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1ccc(S(=O)(=O)CC2CCC(=O)N2C)cc1
Reaction #176274
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)CC(O)c1ccccc1Cl
Reaction #176338
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(CC(=O)C1CC1)c1ccc(Br)cc1
Reaction #176452
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=[N+]([O-])c1ccc(F)cc1OCCCl
Reaction #176666
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=Cc1ccc(C(F)(F)F)cc1C(F)(F)F
Reaction #176704
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1cc2c(Br)nccc2n1S(=O)(=O)c1ccccc1
Reaction #176964
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=Cc1ccncc1F
Reaction #177439
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)C=C1SC(c2ccccc2)N(CCC(C)C)C1=O
Reaction #177765
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CSc1ccc(-c2ccc(C(F)(F)F)cc2)nc1F
Reaction #177797
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)N1CCC(C#N)(CCCCl)CC1
Reaction #177904
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
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