Recherche de Sous-structure

ClCC(Cl)(Cl)Cl

COc1cccc2[nH]cc(C(=O)C(Cl)(Cl)Cl)c12
Reaction #998
4-methoxy-3-trichloroacetyl-1H-indole
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccc[nH]1)C(Cl)(Cl)Cl
Reaction #1223
2-trichloroacetylpyrrole
DOI: 10.6084/m9.figshare.5104873.v1
Fc1ncc(C23CCCN2CCC3)cc1Cl
Reaction #3423
title compound
Rendement 34.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)c1ncc[nH]1
Reaction #4523
tert-butyloxycarbonylimidazole
DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)OC(Cl)C(Cl)(Cl)Cl
Reaction #4526
1,2,2,2-tetrachloroethyl N-methylcarbamate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H](CC(=O)O)C(=O)O
Reaction #4528
expected acid
Rendement 60.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc2c(c1)C(=CCN1CCN(C)CC1)c1ccccc1CO2
Reaction #5138
methyl 11-[2-(4-methyl-1-piperazinyl)ethylidene]-6,11-dihydrodibenz[b,e]oxepin-2-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)n1ncc(C(=O)O)c1Cl
Reaction #41134
1-tert-butyl-5-chloro-1H-pyrazole-4-carboxylic acid
Rendement 87.6%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](NC(=O)C(Cl)(Cl)Cl)[C@H](Oc1ccc2c(cnn2-c2ccc(F)cc2)c1)c1ccccc1
Reaction #41322
2,2,2-Trichloro-N-[(1R,2S)-1-[1-(4-fluorophenyl)indazol-5-yl]oxy-1-phenyl-propan-2-yl]acetamide
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC[C@H]1c1ncc(-c2ccc(Br)cc2)o1
Reaction #46633
(S)-tert-butyl 2-(5-(4-bromophenyl)oxazol-2-yl)pyrrolidine-1-carboxylate
Rendement 63.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)C1CC(=O)C1(Cl)Cl
Reaction #48666
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
Fc1c(Cl)cccc1/C=C/c1noc(C(Cl)(Cl)Cl)n1
Reaction #50644
(E)-3-(3-chloro-2-fluoro-styryl)-5-trichloromethyl-1,2,4-oxadiazole
Rendement 48.7%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C1CC2=CNC=C3C=C(C#N)OCC1=C32
Reaction #53619
titled compound
Rendement 98.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1csc(Br)n1)C(Cl)(Cl)Cl
Reaction #54479
title compound
Rendement 53.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(c1ccc(O)cc1)c1ccc(O)cc1
Reaction #56002
2,2-Bis(4-Hydroxyphenyl)Propane
DOI: 10.6084/m9.figshare.5104873.v1
COCCN(CC=CCl)C(=O)C(Cl)(Cl)Cl
Reaction #62785
above-named product
Rendement 92.7%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccnc1CCl
Reaction #63725
2-chloromethyl-3-methylpyridine
DOI: 10.6084/m9.figshare.5104873.v1
CCCOc1ccnc(CCl)c1C.Cl
Reaction #63734
2-chloromethyl-3-methyl-4-propoxypyridine hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(C(C)(C)C)ccnc1CCl
Reaction #63737
2-chloromethyl-4-tert-butyl-3-methylpyridine
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccnc(CCl)c1C
Reaction #63740
2-chloromethyl-3,4-dimethylpyridine
DOI: 10.6084/m9.figshare.5104873.v1
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