Teilstruktursuche

1417976

COc1c(Br)cc(F)c([N+](=O)[O-])c1Br
Reaction #61683
1,3-Dibromo-5-fluoro-2-methoxy-4-nitrobenzene
Ausbeute 95.0%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cccc(O)c1Br
Reaction #67497
2-Bromo-3-nitro-phenol
Ausbeute 56.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1c(OC(F)F)cccc1[N+](=O)[O-]
Reaction #67498
2-difluoromethoxy-6-nitrobenzonitrile
Ausbeute 84.6%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1c(F)cc(Br)c(OCCCl)c1Br
Reaction #256102
DOI: 10.1039/C8SC04228D
CC(C)Oc1cccc([N+](=O)[O-])c1Br
Reaction #290038
DOI: 10.1039/C8SC04228D
O=[N+]([O-])c1c(F)cc(Br)c(OCCCl)c1Br
Reaction #486193
white crystalline solid
Ausbeute 97.1%DOI: 10.6084/m9.figshare.5104873.v1
Nc1cc(OCCCl)ccc1F
Reaction #486194
dark solid
Ausbeute 90.2%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc([N+](=O)[O-])c(SC)c1OC
Reaction #513888
3-methylthio-4-nitroveratrole
DOI: 10.6084/m9.figshare.5104873.v1
C[SH]1(=O)NC(N2CCN(C(=O)c3ccco3)CC2)=Nc2cc3c(cc21)OCO3.Cl
Reaction #513895
1-methyl-3-[4-(2-furoyl)piperazino]-6,7-methylenedioxy-1H-1,2,4-benzothiadiazine-1-oxide hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cccc(O)c1Br
Reaction #587182
2-bromo-3-nitrophenol
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #587183
crude product
DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc([N+](=O)[O-])c1N1CCCN(C(=O)OC(C)(C)C)CC1
Reaction #620004
4-(2-methoxy-6-nitrophenyl)-[1,4]diazepane-1-carboxylic acid tert-butyl ester
Ausbeute 28.5%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cccc(O)c1Br
Reaction #635129
2-bromo-3-nitrophenol
Ausbeute 45.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc([N+](=O)[O-])c1Br
Reaction #635130
2-bromo-3-nitroanisole
Ausbeute 94.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(N)c1Br
Reaction #635131
2-bromo-3 methoxyaniline
Ausbeute 91.0%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cccc(O)c1Br
Reaction #650044
2-bromo-3-nitrophenol
Ausbeute 45.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc([N+](=O)[O-])c1Br
Reaction #650045
2-bromo-3-nitroanisole
Ausbeute 94.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(N)c1Br
Reaction #650046
2-bromo-3 methoxyaniline
Ausbeute 91.0%DOI: 10.6084/m9.figshare.5104873.v1
Brc1c(OCC2CC2)ccc2cc[nH]c12
Reaction #720759
title compound
Ausbeute 51.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)/C(=C/c1cccc(OCC2CC2)c1Br)N=[N+]=[N-]
Reaction #720761
title compound
Ausbeute 28.0%DOI: 10.6084/m9.figshare.5104873.v1
Seite 1Weiter