Substructure Search

705683

CCOC(=O)N1CCN(c2c(F)cc([N+](=O)[O-])c(F)c2CO)CC1
Reaction #389650
DOI: 10.1039/C8SC04228D
CCOC(=O)N1CCN(c2c(F)cc([N+](=O)[O-])c(F)c2C)CC1
Reaction #890293
DOI: 10.1039/C8SC04228D
CCOC(=O)N1CCN(c2c(F)cc([N+](=O)[O-])c(F)c2CCl)CC1
Reaction #915494
DOI: 10.1039/C8SC04228D
CCOC(=O)N1CCN(c2c(F)cc([N+](=O)[O-])c(F)c2CF)CC1
Reaction #1033345
DOI: 10.1039/C8SC04228D
CCOC(=O)N1CCN(c2c(F)cc([N+](=O)[O-])c(F)c2COC)CC1
Reaction #1043757
DOI: 10.1039/C8SC04228D
CCOC(=O)N1CCN(c2c(F)cc([N+](=O)[O-])c(NC3CC3)c2C)CC1
Reaction #1660654
DOI: 10.1039/C8SC04228D
CCOC(=O)N1CCN(c2c(F)cc([N+](=O)[O-])c(F)c2CO)CC1
Reaction #1725847
3,6-difluoro-2-(4-ethoxycarbonyl-1-piperazinyl)-5-nitrobenzyl alcohol
Yield 37.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)N1CCN(c2c(F)cc([N+](=O)[O-])c(F)c2CCl)CC1
Reaction #1725848
2-(4-ethoxycarbonyl-1-piperazinyl)-3,6-difluoro-5-nitrobenzyl chloride
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)N1CCN(c2c(F)cc([N+](=O)[O-])c(F)c2C)CC1
Reaction #1725849
2-(4-ethoxycarbonyl-1-piperazinyl)-3,6-difluoro-5-nitrotoluene
Yield 96.8%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)N1CCN(c2c(F)cc([N+](=O)[O-])c(NC3CC3)c2C)CC1
Reaction #1725850
N-cyclopropyl-2-methyl-3-(4-ethoxycarbonyl-1-piperazinyl)-4-fluoro-6-nitroaniline
Yield 93.7%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)N1CCN(c2c(F)cc([N+](=O)[O-])c(F)c2CF)CC1
Reaction #1725853
2,5-difluoro-3-fluoromethyl-4-(4-ethoxycarbonyl-1-piperazinyl)nitrobenzene
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)N1CCN(c2c(F)cc([N+](=O)[O-])c(F)c2COC)CC1
Reaction #1725855
3-methoxymethyl-2,5-difluoro-4-(4-ethoxycarbonyl-1-piperazinyl)nitrobenzene
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)N1CCN(c2c(F)cc([N+](=O)[O-])c(F)c2CO)CC1
Reaction #1809466
3,6-difluoro-2-(4-ethoxycarbonyl-1-piperazinyl)-5-nitrobenzyl alcohol
Yield 37.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)N1CCN(c2c(F)cc([N+](=O)[O-])c(F)c2C)CC1
Reaction #1809467
2-(4-ethoxycarbonyl-1-piperazinyl)-3,6-difluoro-5-nitrotoluene
Yield 96.8%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)N1CCN(c2c(F)cc([N+](=O)[O-])c(NC3CC3)c2C)CC1
Reaction #1809468
N-cyclopropyl-2-methyl-3-(4-ethoxycarbonyl-1-piperazinyl)-4-fluoro-6-nitroaniline
Yield 93.7%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)N1CCN(c2c(F)cc([N+](=O)[O-])c(F)c2CO)CC1
Reaction #2194772
3,6-difluoro-2-(4-ethoxycarbonyl-1-piperazinyl)-5-nitrobenzyl alcohol
Yield 37.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)N1CCN(c2c(F)cc([N+](=O)[O-])c(F)c2CCl)CC1
Reaction #2194773
2-(4-ethoxycarbonyl-1-piperazinyl)-3,6-difluoro-5-nitrobenzyl chloride
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)N1CCN(c2c(F)cc([N+](=O)[O-])c(F)c2C)CC1
Reaction #2194774
2-(4-ethoxycarbonyl-1-piperazinyl)-3,6-difluoro-5-nitrotoluene
Yield 96.8%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)N1CCN(c2c(F)cc([N+](=O)[O-])c(NC3CC3)c2C)CC1
Reaction #2194775
N-cyclopropyl-2-methyl-3-(4-ethoxycarbonyl-1-piperazinyl)-4-fluoro-6-nitroaniline
Yield 93.7%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)N1CCN(c2c(F)cc([N+](=O)[O-])c(F)c2CO)CC1
Reaction #2439082
3,6-difluoro-2-(4-ethoxycarbonyl-1-piperazinyl)-5-nitrobenzyl alcohol
Yield 37.3%DOI: 10.6084/m9.figshare.5104873.v1
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