octadecylamine

CCCCCCCCCCCCCCCCCCNc1nc(NCCCCCCCCCCCCCCCCCC)nc(NCCCCCCCCCCCCCCCCCC)n1
Reaction #68702
N,N′,N″-trioctadecyl-1,3,5-triazine-2,4,6-triamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCCCCCCCCCCCCCCCCCn1ccccc1=O
Reaction #79474
N-stearyl pyridone
Выход 87.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CCCCCCCCCCCCCCCCCCN(CCC#N)CCC#N
Reaction #161895
target compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCCCCCCCC=CCCCCCCCC(=O)N(CCCCCCCCCCCCCCCCCC)C1OC(CF)C(O)C(O)C1O
Reaction #198933
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCCCCCCCCCCCCCCCNS(=O)(=O)NCCC
Reaction #212236
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCCCCCCCCCCCCCCCNC1OC(CO)C(O)C(O)C1O
Reaction #212646
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCCCCCCCCCCCCCCCNCC(O)CO
Reaction #216076
white solid
Выход 95.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11
CCCCCCCCCCCCCCCCCCc1ccc[nH]c1=O
Reaction #217448
beige powder
Выход 65.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
CCCCCCCCCCCCCCCCCCNC(=O)c1ccccc1I
Reaction #248717
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCCCCCCCCCCCCCCCCNc1nc(N)nc(N)n1
Reaction #279920
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCCCCCCCCCCCCCCCCCNCC(O)CO
Reaction #298629
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCCCCCCCCCCCCCCCCCN1CCCC1=O
Reaction #299880
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCCCCCCCCCCCCCCCCCNC(=O)c1ccccc1
Reaction #310431
crystals
Выход 83.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_10
CCCCCCCCCCCCCCCCCCNC(=O)c1ccccc1N
Reaction #323095
Anthranilic acid stearylamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_02
CCCCCCCCCCCCCCCCCCN[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O
Reaction #343051
N-octadecyl-β-D-glucopyranosylamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_10
CCCCCCCCCCCCCCCCCCNC1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O
Reaction #343052
N-Octadecyl-D-glucopyranosylamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_10
CCCCCCCCCCCCCCCCCCNS(N)(=O)=O
Reaction #384999
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCCCCCCCCCCCCCCCCCn1ccccc1=O
Reaction #440856
N-stearyl pyridone
Выход 87.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_06
—
Reaction #442211
crystals
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1983_03
C=CC(=O)NCCCCCCCCCCCCCCCCCC
Reaction #451857
N-stearylacrylamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_08
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