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CCOC(=O)c1ccc(F)cc1

CCOC(=O)c1cc(F)c(F)c(OC)c1F
Reaction #10369
title compound
Ausbeute 98.8%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc(OC)c(F)c(F)c1F
Reaction #10371
title compound
Ausbeute 96.8%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc(F)c(F)c(C=NOCc2ccccc2)c1F
Reaction #10374
title compound
Ausbeute 53.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc(F)c(N2CCC(NC(=O)OC(C)(C)C)C2)c(OC)c1F
Reaction #10380
title compound
Ausbeute 77.6%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(F)cc1N
Reaction #66437
ethyl 2-amino-4-fluorobenzoate
Ausbeute 94.0%DOI: 10.6084/m9.figshare.5104873.v1
O=c1nc[nH]c2cc(F)ccc12
Reaction #66438
7-fluoro-3-hydroquinazolin-4-one
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(F)c([N+](=O)[O-])c1
Reaction #68390
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(C(C(=O)NCc2ccc(F)c(F)c2)C(=O)C(C)(C)C)c([N+](=O)[O-])c1
Reaction #68391
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc(NN)c(F)cc1Cl
Reaction #76762
ethyl 2-chloro-4-fluoro-5-hydrazinobenzoate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc([N+](=O)[O-])c(F)cc1Cl
Reaction #76764
ethyl 2-chloro-4-fluoro-5-nitrobenzoate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc(N)c(F)cc1Cl
Reaction #76765
ethyl 5-amino-2-chloro-4-fluorobenzoate
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc(NN)c(F)cc1Cl.Cl
Reaction #76766
ethyl 2-chloro-4-fluoro-5-hydrazinobenzoate hydrochloride
Ausbeute 116.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc(NN)c(F)cc1Cl
Reaction #76767
ethyl 2-chloro-4-fluoro-5-hydrazinobenzoate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(F)c(NC(=O)COC)c1
Reaction #78483
crude product
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(-n2ccnc2C(C)C)c([N+](=O)[O-])c1
Reaction #159939
title compound
Ausbeute 81.7%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(-n2ccnc2C(CC)CC)c([N+](=O)[O-])c1
Reaction #159941
Ethyl 4-[2-(1-ethylpropyl)-1H-imidazol-1-yl]-3-nitrobenzoate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)c1ccc(F)cc1Br
Reaction #166190
title compound
Ausbeute 42.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)c1ccc(F)c(C=O)c1Br
Reaction #166191
title compound
Ausbeute 62.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc([N+](=O)[O-])c(F)cc1F
Reaction #177243
DOI: 10.1039/C8SC04228D
COC(=O)C(C)=CNC(=O)Nc1cc(C(=O)OC(C)C)c(Cl)cc1F
Reaction #181152
DOI: 10.1039/C8SC04228D
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