Teilstruktursuche

1173343

CCCCCCCCCCCCCCCCCCN(CCCCCCCCCCCCCCCCCC)c1ccc([N+](=O)[O-])cc1[N+](=O)[O-]
Reaction #3029
N,N-dioctadecyl-2,4-dinitrobenzenamine
Ausbeute 87.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CCCCCCCCCCSC(c1ccccc1)(c1ccccc1)c1ccccc1)NCCOCCOCCNC(=O)CNc1ccc([N+](=O)[O-])cc1[N+](=O)[O-]
Reaction #46039
6
Ausbeute 79.0%DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)c1ccc(N=Nc2c(C#N)cc([N+](=O)[O-])cc2[N+](=O)[O-])c(NC(C)=O)c1
Reaction #55955
2-Cyano-4,6-dinitro-2'-acetylamino-4'-(N,N-diethylamino)azobenzene
Ausbeute 88.0%DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)c1ccc(N=Nc2c(C#N)cc([N+](=O)[O-])cc2[N+](=O)[O-])c(NC(C)=O)c1
Reaction #55957
2-cyano-4,6-dinitro-2'-acetylamino-4'-(N,N-diethylamino)azobenzene
Ausbeute 83.5%DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)c1ccc(N=Nc2c(C#N)cc([N+](=O)[O-])cc2[N+](=O)[O-])c(NC(C)=O)c1
Reaction #55958
2-Cyano-4,6-dinitro-2'-acetylamino-4'-(N,N-diethylamino)azobenzene
Ausbeute 95.0%DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)c1ccc(N=Nc2c(C#N)cc([N+](=O)[O-])cc2[N+](=O)[O-])c(NC(C)=O)c1
Reaction #55959
2-Cyano-4,6-dinitro-2'-acetylamino-4'-(N,N-diethylamino)azobenzene
Ausbeute 96.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccc([N+](=O)[O-])cc1[N+](=O)[O-])c1cc([N+](=O)[O-])cc([N+](=O)[O-])c1
Reaction #62532
2',3,4',5-tetranitrobenzanilide
Ausbeute 8.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C[C@H](NC(=O)CNC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H]1CCCN1c1ccc([N+](=O)[O-])cc1[N+](=O)[O-])C(=O)N[C@@H](C)C(=O)NCC(=O)N[C@@H](CCC(N)=O)C(=O)N[C@H](CCCNC(=N)N[N+](=O)[O-])C(=O)OCc1ccccc1
Reaction #75312
DNP-Pro-Gln-Gly-Leu-Ala-Gly-Gln-D-Arg(NO2)-OBzl
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H](C)[C@H](Nc1ccc([N+](=O)[O-])cc1[N+](=O)[O-])C(=O)N[C@@H](C)C(=O)NCC(=O)N[C@H](CCCNC(=N)N[N+](=O)[O-])C(=O)OCc1ccccc1
Reaction #75313
DNP-Ile-Ala-Gly-D-Arg(NO2)-OBzl
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CCNc1ccc([N+](=O)[O-])cc1[N+](=O)[O-]
Reaction #82439
solid
Ausbeute 77.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N1CCN(c2ccc(N)c([N+](=O)[O-])c2)CC1
Reaction #86472
title compound
Ausbeute 115.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #170650
( 23 )
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCCCN1C(=O)C(C)(C)c2cc(NC(=O)CCc3ccccc3)c([N+](=O)[O-])cc21
Reaction #181302
DOI: 10.1039/C8SC04228D
CS(=O)(=O)OCCN(CCOS(C)(=O)=O)c1c(C(=O)NCC(O)CO)cc([N+](=O)[O-])cc1[N+](=O)[O-]
Reaction #185446
DOI: 10.1039/C8SC04228D
CC(C)(C)Nc1c([N+](=O)[O-])cc([N+](=O)[O-])c2nc(C(F)(F)F)[nH]c12
Reaction #189259
DOI: 10.1039/C8SC04228D
COc1ccc(C(=O)Nc2cc3c(cc2[N+](=O)[O-])NC(=O)C3(C)C)cc1
Reaction #199952
DOI: 10.1039/C8SC04228D
Cc1cc(N2CCOCC2)cc([N+](=O)[O-])c1N
Reaction #200403
DOI: 10.1039/C8SC04228D
O=C(O)CCNc1ccc([N+](=O)[O-])cc1[N+](=O)[O-]
Reaction #225302
DOI: 10.1039/C8SC04228D
CNc1ccc([N+](=O)[O-])cc1N
Reaction #225529
DOI: 10.1039/C8SC04228D
Cc1cc(N)c([N+](=O)[O-])cc1NC(=O)OCCCl
Reaction #232452
DOI: 10.1039/C8SC04228D
Seite 1Weiter