1,2-epoxyoctadecane

CCCCCCCCCCCCCCCCC(O)CNCCO
Reaction #1204
title compound
Ausbeute 74.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCCCCCCCCCCCCCC(O)CN(C)CCO
Reaction #1205
title compound
Ausbeute 67.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCCCCCCCCCCCCCC(O)CN
Reaction #1218
title compound
Ausbeute 83.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCCCCCCCCCCCCCC(O)CNCCO
Reaction #379079
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CC(O)CO.OCCCCCCCCCCCCCCCCCCOCCO
Reaction #809179
1,2-propanediol monohydroxyoctadecyl ether
Ausbeute 96.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_11
O=C1C=C(Cl)C(=O)O1
Reaction #926953
chloromaleic anhydride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_06
CCCCCCCCCCCCCCCCC(O)CN(C)CCO
Reaction #1297360
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (5/10)
CCCCCCCCCCCCCCCCC(O)CN
Reaction #1647185
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (1/10)
—
Reaction #1684903
alkoxylated alcohol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_04