Teilstruktursuche

1412646

CC(COc1cccc(Cl)[n+]1[O-])CC(C)(C)C
Reaction #49969
2-chloro-6-(2,4,4-trimethypentyloxy) pyridine N-oxide
DOI: 10.6084/m9.figshare.5104873.v1
CC(CCOc1cccc(Cl)[n+]1[O-])CC(C)(C)C
Reaction #49970
2-chloro-6-(3,5,5trimethylhexyloxy)pyridine N-oxide
DOI: 10.6084/m9.figshare.5104873.v1
[OH-]
Reaction #49971
hydroxide
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCSc1cccc(Cl)[n+]1[O-]
Reaction #49972
2-chloro-6-octylthiopyridine N-oxide
DOI: 10.6084/m9.figshare.5104873.v1
[O-][n+]1c(Cl)cccc1-c1cccs1
Reaction #49973
2-chloro-6-thiophenylpyridine N-oxide
DOI: 10.6084/m9.figshare.5104873.v1
[O-][n+]1c(Cl)cccc1Oc1ccccc1
Reaction #49974
2-chloro-6-phenyloxypyridine N-oxide
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(Cl)[n+]([O-])c(Cl)c1C(=O)O
Reaction #178729
DOI: 10.1039/C8SC04228D
CC(CCOc1cccc(Cl)[n+]1[O-])CC(C)(C)C
Reaction #179804
DOI: 10.1039/C8SC04228D
[O-][n+]1c(Cl)cccc1Cl
Reaction #201294
DOI: 10.1039/C8SC04228D
C[N+](C)([O-])C(=O)Nc1ccc(Oc2cccc(Cl)n2)cc1
Reaction #524463
N'-(4-((6-chloro-2-pyridinyl)oxy)phenyl)-N,N-dimethyl urea-1-oxide
DOI: 10.6084/m9.figshare.5104873.v1
C[N+](C)([O-])C(=O)Nc1ccc(Oc2cccc(Cl)n2)cc1
Reaction #548768
N'-(4-((6-chloro-2-pyridinyl)oxy)phenyl)-N,N-dimethyl urea-1-oxide
DOI: 10.6084/m9.figshare.5104873.v1
OC1CCCCC1
Reaction #698994
cyclohexanol
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCOc1cccc(Cl)[n+]1[O-]
Reaction #1217505
DOI: 10.1039/C8SC04228D
[O-][n+]1c(Cl)cccc1Cl
Reaction #1277992
light yellow solid
Ausbeute 87.7%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cc(Cl)nc(Cl)c1
Reaction #1277993
yellow solid
Ausbeute 66.4%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cc(Cl)nc(Cl)c1
Reaction #1349966
2,6-Dichloro-4-nitropyridine
DOI: 10.6084/m9.figshare.5104873.v1
C[N+](C)([O-])C(=O)Nc1ccc(Oc2cccc(Cl)n2)cc1
Reaction #1502268
N'-(4-((6-chloro-2-pyridinyl)oxy)phenyl)-N,N-dimethyl urea-1-oxide
DOI: 10.6084/m9.figshare.5104873.v1
C[N+](C)([O-])C(=O)Nc1ccc(Oc2cccc(Cl)n2)cc1
Reaction #1502275
N'-(4-((6-chloro-2-pyridinyl)oxy)phenyl)-N,N-dimethyl urea-1-oxide
DOI: 10.6084/m9.figshare.5104873.v1
[O-][n+]1c(Cl)cccc1Cl
Reaction #1524920
compound
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(COc1cccc(Cl)[n+]1[O-])CC(C)(C)C
Reaction #1575907
2-chloro-6-(2,4,4-trimethypentyloxy)pyridine N-oxide
DOI: 10.6084/m9.figshare.5104873.v1
Seite 1Weiter