cyclohexadecanolide

O=C(CCCCCCCCCCCCCCCO)N(CCO)CCO
Reaction #1210
N,N-bis(2-hydroxyethyl)-16-hydroxyhexadecanamide
Ausbeute 82.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
OCCNCCCCCCCCCCCCCCCCOC1CCCCO1
Reaction #1212
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
OCCCCCCCCCCCCCCCCO
Reaction #613470
Hexadecane-1,16-diol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
CON(C)C(=O)CCCCCCCCCCCCCCCO
Reaction #727117
N-methoxy-N-methyl-16-hydroxyhexadecanamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_04
CON(C)C(=O)CCCCCCCCCCCCCCCO
Reaction #727119
N-methoxy-N-methyl-16-hydroxyhexadecanamide
Ausbeute 89.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_04
O=C(O)CCCCCCCCCCCCCCCI
Reaction #1366316
16-Iodohexadecanoic Acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_09
O=C(O)CCCCCCCCCCCCCCCO
Reaction #1528327
16-hydroxy hexadecanoic acid
Ausbeute 97.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_03
COC(=O)CCCCCCCCCCCCCCCO
Reaction #1637592
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (1/10)
O=C(O)CCCCCCCCCCCCCCCO
Reaction #2244849
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (4/10)
COC(=O)CCCCCCCCCCCCCCCO
Reaction #2347252
methyl 16-hydroxyhexadecanoate
Ausbeute 90.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_12