Recherche de Sous-structure

249793

CC1(C)CCC(Br)c2cc(Br)ccc21
Reaction #1310
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CCC(OC2CCCCC2)c2cc(Br)ccc21
Reaction #1311
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CCC(Br)c2cc(Br)ccc21
Reaction #1316
Compound I
DOI: 10.6084/m9.figshare.5104873.v1
CC(=S)C1CCC(C)(C)c2ccc(Br)cc21
Reaction #1317
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOc1ccc(C2(Br)C=CC=CC2)c(F)c1F
Reaction #7430
formula 13
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCC(OC)C(Br)c1ccccc1
Reaction #46729
1-Bromo-2-methoxy-nonyl benzene
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCc1ccc(C(=O)O)c(OC)c1
Reaction #46730
pure product
Rendement 20.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=C(c2ccccc2)c2ccc(OC)cc2C1Br
Reaction #47824
titled compound
Rendement 74.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=C(c2ccccc2)c2ccc(OC)cc2C1OC
Reaction #47825
titled compound
Rendement 24.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=C(c2ccccc2)c2ccc(OC)cc2C1OCC
Reaction #47826
titled compound
Rendement 52.0%DOI: 10.6084/m9.figshare.5104873.v1
CCNC1C(C(=O)OCC)=C(c2ccccc2)c2ccc(OC)cc21
Reaction #47841
titled compound
Rendement 75.6%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=C(c2ccccc2)c2ccc(OC)cc2C1N1CCOCC1
Reaction #47842
titled compound
Rendement 83.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=C(c2ccccc2)c2ccc(OC)cc2C1NCc1ccccc1
Reaction #47843
titled compound
Rendement 44.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=C(c2ccccc2)c2ccc(OC)cc2C1NC1CCCCC1
Reaction #47844
titled compound
Rendement 24.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CC=Cc1cccc(OCc2c(C)cccc2C)c1
Reaction #53313
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OC(C)(CCO)c1ccc(-c2ccc(F)cc2F)cc1
Reaction #55213
3-acetoxy-3-(2',4'-difluoro-4-biphenylyl)butan-1-ol
DOI: 10.6084/m9.figshare.5104873.v1
BrC(Cc1ccccc1)c1ccccc1
Reaction #69599
title product
Rendement 84.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C(=Cc2ccc(Cl)cc2)C(Br)c2ccccc21
Reaction #87293
14a
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(C=C2C(=O)c3ccccc3C2Br)cc1
Reaction #87294
15a
DOI: 10.6084/m9.figshare.5104873.v1
O=C1C(=Cc2ccccc2)C(NC2CCCCCC2)c2ccccc21
Reaction #87295
5
Rendement 82.0%DOI: 10.6084/m9.figshare.5104873.v1
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