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Cc1cccc2ccc(Cl)cc12

COC(=O)CC(=O)CC(O)CCc1c(C)cc(Cl)c2ccc(Cl)cc12
Reaction #189038
DOI: 10.1039/C8SC04228D
Cc1cc(Cl)c2ccc(Cl)cc2c1CCC=O
Reaction #197405
DOI: 10.1039/C8SC04228D
Cl.Cl.O=Cc1c2ccccc2c(C=O)c2cc(Cl)ccc12
Reaction #215253
2-chloro-9,10-anthracenedicarboxaldehyde dihydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
Clc1ccc2cccc(CBr)c2c1
Reaction #255160
DOI: 10.1039/C8SC04228D
Clc1cc(Cl)c2cccc3c2c1N=C3NCCCn1ccnc1
Reaction #279307
DOI: 10.1039/C8SC04228D
O=Cc1c2ccccc2cc2ccc(Cl)cc12
Reaction #345498
2-chloro-9-formylanthracene
Ausbeute 56.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OC1CC2c3ccccc3C1(C=O)c1cc(Cl)ccc12
Reaction #345499
title compound
Ausbeute 463.8%DOI: 10.6084/m9.figshare.5104873.v1
C=CCON1C(=O)c2ccc(Cl)c3c(N4CCCC4)cc(Cl)c(c23)C1=O
Reaction #366167
title compound
Ausbeute 90.3%DOI: 10.6084/m9.figshare.5104873.v1
C=CCON1C(=O)c2ccc(Cl)c3c(N4CC[C@H](NC(=O)OC(C)(C)C)C4)cc(Cl)c(c23)C1=O
Reaction #366168
title compound
Ausbeute 57.6%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccc(Cl)c3c(N4CCCC4)cc(Cl)c(c23)C(=O)N1O
Reaction #366224
title compound
Ausbeute 43.8%DOI: 10.6084/m9.figshare.5104873.v1
Cl.N[C@H]1CCN(c2cc(Cl)c3c4c(ccc(Cl)c24)C(=O)N(O)C3=O)C1
Reaction #366225
(S)-6-(3-Aminopyrrolidin-1-yl)-4,7-dichloro-2-hydroxy-1H-benzo[de]iso quinoline-1,3-dione hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CC(O)CC(CCc2c(Cl)cc(Cl)c3ccc(Cl)cc23)O1
Reaction #405500
DOI: 10.1039/C8SC04228D
CCc1cccc2c(C=O)cc(Cl)c(OCOC)c12
Reaction #575305
captioned compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1c2c(cc3ccc(Cl)cc13)CCC2
Reaction #600508
naphthalene
DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1c2c(cc3ccc(Cl)cc13)CCC2
Reaction #600517
naphthalene
Ausbeute 83.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1c2c(cc3ccc(N(C)C)cc13)CCC2
Reaction #600526
solid
Ausbeute 70.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=O)c1c(C)cc2ccc(Cl)cc2c1-c1ccc(Cl)cc1
Reaction #601335
Ethyl 2-(7-chloro-1-(4-chlorophenyl)-3-methylnaphthalen-2-yl)-2-oxoacetate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(O)c1c(C)cc2ccc(Cl)cc2c1-c1ccc(Cl)cc1
Reaction #601336
title compound
Ausbeute 107.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(OC(C)(C)C)c1c(C)cc2ccc(Cl)cc2c1-c1ccc(Cl)cc1
Reaction #601337
Ethyl 2-tert-butoxy-2-(7-chloro-1-(4-chlorophenyl)-3-methylnaphthalen-2-yl)acetate
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc2ccc(Cl)cc2c(-c2ccc(Cl)cc2)c1C(OC(C)(C)C)C(=O)O
Reaction #601338
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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