Teilstruktursuche

CCCCCCBr

COC(=O)c1cc(-c2ccc(OC)c(F)c2)nn(CC2CCCC2)c1=O
Reaction #8098
title compound
Ausbeute 72.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC1=C(C)CCC1O
Reaction #9397
2-ethyl-3-methyl-cyclopent-2-enol
DOI: 10.6084/m9.figshare.5104873.v1
BrCCCCCCC1CCCCC1
Reaction #9908
(6-bromo-hexyl)-cyclohexane
Ausbeute 89.0%DOI: 10.6084/m9.figshare.5104873.v1
Br.CN1CCC[C@H]1c1ccc[n+](CCCCCCC2CCCCC2)c1.[Br-]
Reaction #9909
(S)-1-(6-cyclohexyl-hexyl)-3-(1-methyl-pyrrolidin-2-yl)-pyridinium bromide hydrobromide salt
Ausbeute 63.3%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(C(=O)OC(C)(C)C)C[C@H]2Cc3ccc(COCC4CCCCC4)nc3N21
Reaction #12036
(4R,9aR)-6-Cyclohexylmethoxymethyl-4-methyl-3,4,9,9a-tetrahydro-1H-2,4a,5-triaza-fluorene-2-carboxylic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(Nc3c(Cl)cncc3Cl)cc(=O)oc2c1OCCC1CCCCC1
Reaction #48947
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCCCCCCCOc1ccc(C(=O)OC)cc1
Reaction #49716
Methyl 4-docosyloxybenzoate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(C)(OCC)P(=O)(CC1CCCCC1)OCC
Reaction #50055
1,1-diethoxyethyl(cyclohexylmethyl)phosphinic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)OB(O)c1ccc(CCCCCCCCCCCO)cc1
Reaction #53274
desired product
DOI: 10.6084/m9.figshare.5104873.v1
N[C@H]1CC[C@H](CCCCCBr)CC1
Reaction #53928
trans-4-(5-Bromo-pentyl)-cyclohexylamine
Ausbeute 129.2%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(N[C@H]1CC[C@H](CCCCCBr)CC1)c1ccc(C(F)(F)F)cc1
Reaction #53929
trans-N-[4-(5-Bromo-pentyl)-cyclohexyl]-4-trifluoromethyl-benzenesulfonamide
Ausbeute 91.0%DOI: 10.6084/m9.figshare.5104873.v1
Br.CN[C@H]1CC[C@H](CCCCCBr)CC1
Reaction #53935
trans-[4-(5-Bromo-pentyl)-cyclohexyl]-methyl-amine hydrobromide
Ausbeute 179.2%DOI: 10.6084/m9.figshare.5104873.v1
C/C=C/COC(C)C1=CC(C)(C)Nc2ccc(-c3ccccc3OC)cc21
Reaction #54065
title compound
Ausbeute 101.0%DOI: 10.6084/m9.figshare.5104873.v1
C/C=C/COC(C)C1=CC(C)(C)Nc2ccc(-c3ccccc3OC)cc21
Reaction #54066
title compound
Ausbeute 25.6%DOI: 10.6084/m9.figshare.5104873.v1
Nc1nc(Cl)cc(-c2cc(Cl)ccc2OCC2CCCCC2)n1
Reaction #56930
4-chloro-6-(5-chloro-2-cyclohexylmethoxy-phenyl)-pyrimidin-2-ylamine
Ausbeute 20.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC1=C(C)CCC1O
Reaction #57037
2-ethyl-3-methyl-cyclopent-2-enol
DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)N1OCC1CCCCC1
Reaction #57437
2-(cyclohexylmethoxy)-1H-isoindole-1,3(2H)-dione
DOI: 10.6084/m9.figshare.5104873.v1
N#CCCCCCOCCCc1ccc(OCCCCCC#N)cc1
Reaction #61066
6-{3-[4-(5-cyanopentyloxy)phenyl]propoxy}hexanenitrile
Ausbeute 30.0%DOI: 10.6084/m9.figshare.5104873.v1
N#CCCCCCOc1cccc(CN2CCCCC2)c1
Reaction #63871
6-(3-piperidinomethylphenoxy)hexanenitrile
DOI: 10.6084/m9.figshare.5104873.v1
CCCCC[C@H]1CC[C@H](CCCOc2ccc(C=O)cc2)CC1
Reaction #64066
4-[3-(trans-4-pentylcyclohexyl)-1-propyloxy]benzaldehyde
Ausbeute 121.9%DOI: 10.6084/m9.figshare.5104873.v1
Seite 1Weiter