6-amino-1-hexanol

CCC(C)NC(=O)CC(NCCCCCCO)C(=O)OC
Reaction #42627
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C(O)c1ccc2c(c1)C(=O)N(CCCCCCO)C2=O
Reaction #65308
1,3-Dioxo-2-(6-hydroxyhex-1-yl)-isoindole-5-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
Cc1onc(-c2ccccc2)c1COc1ccc(C(=O)NCCCCCCO)cn1
Reaction #170520
title compound
Ausbeute 20.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(=O)NCCCCCCO
Reaction #181846
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(NCCCCCCO)OCc1ccccc1
Reaction #182083
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CNC(=C[N+](=O)[O-])CCCCCCO
Reaction #207240
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCc1ccc(C(=O)NCCCCCCO)cc1
Reaction #269065
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Cc1ccccc1C(=O)c1ccc(Nc2ccccc2NC(=O)CCC(=O)NCCCCCCO)cc1Cl
Reaction #289910
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=C(NCCCCCCO)Oc1ccc(Oc2ccccc2)cc1
Reaction #347517
solid
Ausbeute 86.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_06
CCC(C)NC(=O)CC(NCCCCCCO)C(=O)OC
Reaction #356896
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_11
COc1ccc(-c2c(-c3ccccc3)oc3ncnc(NCCCCCCO)c23)cc1
Reaction #382345
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCC(C)NC(=O)CC(NCCCCCCO)C(=O)OC
Reaction #382582
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCN(CCCCCCO)c1ccc(C=O)cc1
Reaction #386091
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
Cc1nc(Cl)c([N+](=O)[O-])c(NCCCCCCO)c1C
Reaction #404862
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
O=C(CCCC[C@@H]1SC[C@@H]2NC(=O)N[C@@H]21)NCCCCCCO
Reaction #417552
white crystals
Ausbeute 95.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1990_01
Cc1onc(-c2ccccc2)c1COc1ccc(C(=O)NCCCCCCO)cn1
Reaction #419119
title compound
Ausbeute 20.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
Cc1onc(-c2ccccc2)c1COc1ccc(C(=O)NCCCCCCO)cn1
Reaction #419619
title compound
Ausbeute 20.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
Nc1cc2cccnc2c2ncccc12
Reaction #429093
Compound ( 2 )
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_01
CCCCc1ccc(C(=O)NCCCCCCO)cc1
Reaction #447163
desired product
Ausbeute 85.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1991_03
O=C(NCCCCCCO)OCc1ccccc1
Reaction #463287
6-(N-benzyloxycarbonylamino)hexan-1-ol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_01
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