2-phenylethyl alcohol

BrCCCCCCOCCc1ccccc1
Reaction #5304
title compound
Ausbeute 55.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC(=O)N1CCCC1c1cc2c(cc1OCCc1ccccc1)nc(-c1ccccn1)n2COCC[Si](C)(C)C
Reaction #41551
1-(2-(6-phenethyloxy-2-pyridin-2-yl-3-(2-trimethylsilanyl-ethoxymethyl)-3H-benzimidazol-5-yl)-pyrrolidin-1-yl)-ethanone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCOC(=O)CC(C)=O
Reaction #56050
ethyl acetoacetate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
O=CCc1ccccc1
Reaction #56123
phenylacetaldehyde
Ausbeute 67.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
c1ccc(CCOC2CCCCC2)cc1
Reaction #94989
CYCLOHEXYL PHENETHYLETHER
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
c1ccc(CCOC2CCCCC2)cc1
Reaction #95916
Cyclohexyl Phenethylether
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
O=[N+]([O-])c1cccc(OCCc2ccccc2)c1
Reaction #96074
dark oil
Ausbeute 219.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
O=C1c2ccccc2C(=O)N1CCCc1cccc(OCCc2ccccc2)c1
Reaction #161548
2-(3-(3-phenethoxyphenyl)propyl)isoindoline-1,3-dione
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C(OCCc1ccccc1)C1CCCCC1
Reaction #174901
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
N#CCc1ccc(OCCc2ccccc2)cc1
Reaction #176966
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc(NCCc2ccccc2)cc1
Reaction #182427
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Nc1nc(OCCc2ccccc2)c([N+](=O)[O-])c(-c2ccco2)n1
Reaction #190017
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(=O)N1CCCC1c1cc2c(cc1OCCc1ccccc1)nc(-c1ccccn1)n2COCC[Si](C)(C)C
Reaction #194707
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)CCC(=O)c1ccc(CCO)cc1
Reaction #203237
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc(C(=O)Cc2c(Cl)cncc2Cl)c2c(CC(=O)OCCc3ccccc3)coc12
Reaction #207387
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1ccc(S(=O)(=O)OCCc2ccccc2)cc1
Reaction #210562
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(c1ccccc1C(F)(F)F)N1CCN(c2ccc(OCCc3ccccc3)nn2)CC1
Reaction #229944
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cn1nc(-c2nc(O)c(N)nc2-c2ccccc2)ccc1=O
Reaction #244610
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(NC(=O)Cc1cc(F)cc(F)c1)C(=O)NCC(=O)OCCc1ccccc1
Reaction #244915
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=CCc1ccccc1
Reaction #247941
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
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