Recherche de Sous-structure

Clc1ccccc1

CC(C)(C)OC(=O)c1cc(C(F)(F)F)cc(Cl)c1C(=O)O
Reaction #3225
title compound
Rendement 82.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1C(=O)N(C(=O)Nc2ccccc2)c2ccc(Cl)cc21
Reaction #4577
Methyl 1-N-(phenyl)carbamoyl-5-chlorooxindole-3-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(Cl)cc1OC(C)C(=O)OC
Reaction #50475
desired material
Rendement 102.6%DOI: 10.6084/m9.figshare.5104873.v1
CC1Oc2cc(Cl)ccc2C1=O
Reaction #50476
desired product
Rendement 44.4%DOI: 10.6084/m9.figshare.5104873.v1
NNc1ccc(C(F)(F)F)c(Cl)c1Cl
Reaction #63139
2,3-dichloro-4-trifluoromethyl-phenylhydrazine
Rendement 79.4%DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1ncc(C(C)O)n1Cc1ccccc1Cl
Reaction #65251
2-n-butyl-1-(2-chlorophenyl)methyl-5-(a-hydroxy) ethyl-1H-imidazole
Rendement 92.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(Cl)c(-c2ccc(C(=O)Nc3ccc(N4CCNCC4)cc3)c3nccnc23)c1Cl
Reaction #71332
title compound
Rendement 80.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(Cl)ccc(CNC(=O)C(C)(C)C)c1F
Reaction #87617
product
Rendement 63.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1cc2[nH]c(C(=O)O)nc2cc1C
Reaction #95420
5-Acetyl-6-methyl-benzimidazole-2-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCCC(=O)c1cc2nc(C(=O)O)n(C)c2cc1Cl
Reaction #95423
5-butyryl-6-chloro-1-methyl-benzimidazole-2-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
CC(CCCCl)(C(=O)O)c1ccc(Cl)cc1
Reaction #158273
title compound
Rendement 83.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C(=O)NNC(=O)C(C)(CCCCl)c2ccc(Cl)cc2)ccc1-c1cnc(C)o1
Reaction #158274
title compound
Rendement 82.6%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cncc(-c2cccc(C(=O)CC(=O)Nc3cc(C)c(Cl)cc3NC(=O)OC(C)(C)C)c2)n1
Reaction #176243
DOI: 10.1039/C8SC04228D
CC(=O)N(Cc1cc(C(F)(F)F)cc(C(F)(F)F)c1)C1CCCN(C(=O)OC(C)C)c2cc(Cl)c(C)cc21
Reaction #177688
DOI: 10.1039/C8SC04228D
N#CC1CC1C(O)c1ccc(F)cc1Cl
Reaction #183459
DOI: 10.1039/C8SC04228D
COc1cc(Cl)cc(C(=O)N(CCC(=O)O)C(C)C)c1
Reaction #191055
DOI: 10.1039/C8SC04228D
CN(Cc1ccc(Cl)c(Cl)c1)C(=O)C1=C(O)C(=O)N(CCN2CCCCC2)C1
Reaction #192085
DOI: 10.1039/C8SC04228D
O=Cc1nc(-c2ccccc2Cl)cs1
Reaction #193969
DOI: 10.1039/C8SC04228D
CCOP(=O)(COC(=O)c1ccc(Cl)cc1OC)OCC
Reaction #202502
DOI: 10.1039/C8SC04228D
CN(Cc1ccc(Cl)c(Cl)c1)C(=O)C1=C(O)C(=O)N(CC(=O)O)C1
Reaction #203084
DOI: 10.1039/C8SC04228D
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