Substructure Search

1338

CSC[C@H](Nc1cc(F)ccc1[N+](=O)[O-])C(=O)O
Reaction #972
N-(5-Fluoro-2-nitrophenyl)-S-methyl-L-cysteine
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cc([N+](=O)[O-])c(F)cc1F
Reaction #6959
2,4-difluoro-5-nitrobenzoic acid
Yield 98.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1cc(C(=O)O)c(F)cc1F
Reaction #6960
2,4-difluoro-5-aminobenzoic acid
Yield 97.6%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(C)Nc1ccc(F)c(F)c1F
Reaction #8526
title compound
Yield 97.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C)Nc1ccc(F)c(F)c1F
Reaction #8528
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C)Nc1ccc(F)c(F)c1F
Reaction #8531
title compound
Yield 97.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(Nc1ccc(F)c(F)c1F)C(=O)O
Reaction #8534
title compound
Yield 98.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(Nc1ccc(F)c(F)c1F)C(=O)O
Reaction #8535
title compound
Yield 97.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(Nc1ccc(F)c(F)c1F)C(=O)O
Reaction #8536
title compound
Yield 96.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1CN(C(=O)OCc2ccccc2)CCN1c1cc(F)c(F)cc1[N+](=O)[O-]
Reaction #11907
title compound
Yield 16.7%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccc(Oc2ccc([N+](=O)[O-])c(F)c2F)cn1
Reaction #41610
2,3-difluoro-1-(6-methanesulfonyl-pyridin-3-yloxy)-4-nitro-benzene
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc(Oc2c(F)cccc2F)c(F)c1F
Reaction #41612
2,3-difluoro-1-(2,6-difluoro-phenoxy)-4-nitro-benzene
DOI: 10.6084/m9.figshare.5104873.v1
Cn1c(C(F)(F)F)cc(=O)n(-c2cc(F)c([N+](=O)[O-])cc2F)c1=O
Reaction #43649
2,5-difluoro-4-[3-methyl-2,6-dioxo-4-(trifluoromethyl)-1,2,3,6-tetrahydropyrimidin-1-yl]nitrobenzene
Yield 43.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCNc1cc(F)ccc1[N+](=O)[O-]
Reaction #45926
2-n-butylamino-4-fluoronitrobenzene
DOI: 10.6084/m9.figshare.5104873.v1
CCCCNc1cc(F)cc(OCCCN(CC)CC)c1[N+](=O)[O-]
Reaction #45930
2-n-butylamino-6-(3-diethylaminopropoxy)-4-fluoronitrobenzene
DOI: 10.6084/m9.figshare.5104873.v1
CCCCNc1cc(F)cc(F)c1[N+](=O)[O-]
Reaction #45931
2-butylamino-4,6-difluoronitrobenzene
Yield 130.3%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc(F)cc1Oc1ccccc1O
Reaction #49798
title product
Yield 55.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cc([N+](=O)[O-])c(F)c(Cl)c1F
Reaction #51443
desired product
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cl)c1cc([N+](=O)[O-])c(F)c(Cl)c1F
Reaction #51444
desired product
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cc([N+](=O)[O-])c(F)c(F)c1F
Reaction #60238
clean desired product
Yield 92.0%DOI: 10.6084/m9.figshare.5104873.v1
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