N-Hydroxyphthalimide

O=C1c2ccccc2C(=O)N1OCc1ccccc1CBr
Reaction #9049
title compound
Ausbeute 46.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C(ON1C(=O)c2ccccc2C1=O)c1ccccc1
Reaction #47133
N-benzoyloxyphthalimide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CSCCCON1C(=O)c2ccccc2C1=O
Reaction #49007
2-(3-methylsulfanyl-propoxy)-isoindole-1,3-dione
Ausbeute 65.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCOC(=O)CCCON1C(=O)c2ccccc2C1=O
Reaction #49025
4-(1,3-dioxo-1,3-dihydro-isoindol-2-yloxy)-butyric acid ethyl ester
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
[O-]O.c1ccc(C2CCCCC2)cc1
Reaction #52105
1-cyclohexylbenzene hydroperoxide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CC(C)(O)c1ccccc1
Reaction #52106
2-phenyl-2-propanol
Ausbeute 13.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
OOCc1ccccc1
Reaction #52107
Benzyl hydroperoxide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
OC1CCCCCCCCCCCCCC1
Reaction #52108
Cyclopentadecanol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
OC1CCCCCCCCCCCCCC1
Reaction #52109
Cyclopentadecanol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
OC1CCCCCCC1
Reaction #52110
Cyclooctanol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
OC1CCCCCCC1
Reaction #52111
Cyclooctanol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
OC1CCCCCCCCCCC1
Reaction #52112
Cyclododecanol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
OC1CCCCCCCCCCC1
Reaction #52113
Cyclododecanol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CCOC(=O)CC(c1ccccc1)n1ccc2cc(OCCON3C(=O)c4ccccc4C3=O)ccc21
Reaction #52272
title compound
Ausbeute 96.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
O=C1c2ccccc2C(=O)N1OC1CCCC1
Reaction #57429
2-(cyclopentyloxy)-1H-isoindole-1,3(2H)-dione
Ausbeute 80.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CCC(C)ON1C(=O)c2ccccc2C1=O
Reaction #57436
yellow solid
Ausbeute 89.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
O=C1c2ccccc2C(=O)N1OCC1CCCCC1
Reaction #57437
2-(cyclohexylmethoxy)-1H-isoindole-1,3(2H)-dione
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
O=C1c2ccccc2C(=O)N1OC1CCOCC1
Reaction #57440
2-(tetrahydro-2H-pyran-4-yloxy)-1H-isoindole-1,3(2H)-dione
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
O=C1c2ccccc2C(=O)N1OC1CCCCC1
Reaction #57446
2-(cyclohexyloxy)-1H-isoindole-1,3(2H)-dione
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
O=C1c2ccccc2C(=O)N1OC1CCCCC1
Reaction #57478
2-(cyclohexyloxy)-1H-isoindole-1,3(2H)-dione
Ausbeute 75.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
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