Ähnlichkeitssuche

9950

COC(=O)c1cccc([N+](=O)[O-])c1N(Cc1ccc(-c2ccccc2C(N)=O)cc1)C(=O)OC(C)(C)C
Reaction #5335
syrup
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1
CNc1c(C(=O)OC)cccc1[N+](=O)[O-]
Reaction #52186
Methylamino-3-nitro-benzoic acid-methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cccc([N+](=O)[O-])c1NC(C)C
Reaction #65144
Ethyl 2-[(1-methylethyl)amino]-3-nitrobenzoate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cccc([N+](=O)[O-])c1N(Cc1ccc(-c2ccccc2-c2nnnn2Cc2ccc(OC)cc2)cc1)C(=O)OC(C)(C)C
Reaction #70073
methyl 2-(N-tert-butoxycarbonyl-N-{(2′-[1-(p-methoxybenzyl)-1H-tetrazol-5-yl]biphenyl-4-yl)methyl}amino)-3-nitrobenzoate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cccc([N+](=O)[O-])c1N(Cc1ccc(-c2ccccc2-c2nnnn2Cc2ccccc2)cc1)C(=O)OC(C)(C)C
Reaction #70076
methyl 2-(N-tert-butoxycarbonyl-N-{(2′-[1-benzyl-1H-tetrazol-5-yl]biphenyl-4-yl)methyl}amino)-3-nitrobenzoate
Ausbeute 81.7%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cccc([N+](=O)[O-])c1Br
Reaction #79591
methyl 2-bromo-3-nitrobenzoate
Ausbeute 96.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cccc(N)c1Br
Reaction #79592
methyl 2-bromo-3-aminobenzoate
Ausbeute 99.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cccc([N+](=O)[O-])c1Br
Reaction #79610
methyl 2-bromo-3-nitrobenzoate
Ausbeute 96.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cccc(N)c1Br
Reaction #79611
methyl 2-bromo-3-aminobenzoate
Ausbeute 99.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cccc([N+](=O)[O-])c1Br
Reaction #79625
methyl 2-bromo-3-nitrobenzoate
Ausbeute 96.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cccc(N)c1Br
Reaction #79626
methyl 2-bromo-3-aminobenzoate
Ausbeute 99.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cccc(N)c1Br
Reaction #79627
methyl 2-bromo-3-aminobenzoate
Ausbeute 99.2%DOI: 10.6084/m9.figshare.5104873.v1
CCCC(=O)Nc1c(N)cccc1C(=O)OC
Reaction #190582
DOI: 10.1039/C8SC04228D
COC(=O)c1cccc(N)c1Br
Reaction #234139
DOI: 10.1039/C8SC04228D
COC(=O)c1ccc(-c2ccccc2NC(=O)OC(C)(C)C)cc1[N+](=O)[O-]
Reaction #251288
DOI: 10.1039/C8SC04228D
COC(=O)c1cccc(N)c1Br
Reaction #259134
DOI: 10.1039/C8SC04228D
COC(=O)c1cccc([N+](=O)[O-])c1N(Cc1ccc(-c2ccccc2-c2nnnn2Cc2ccc(OC)cc2)cc1)C(=O)OC(C)(C)C
Reaction #264174
DOI: 10.1039/C8SC04228D
COC(=O)c1cccc([N+](=O)[O-])c1N(C)C(=O)C(F)(F)F
Reaction #267763
DOI: 10.1039/C8SC04228D
COC(=O)c1cccc([N+](=O)[O-])c1F
Reaction #282518
DOI: 10.1039/C8SC04228D
COC(=O)c1cccc([N+](=O)[O-])c1F
Reaction #326434
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Seite 1Weiter