1-dodecanol

C[C@@H]1OC(=O)[C@H](C)OC1=O.O=C1CCCCCO1
Reaction #2354
ε-CAPROLACTONE L-LACTIDE
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
C=C(C)C(=O)OCCCCCCCCCCCC
Reaction #4991
Dodecyl Methacrylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCCCCCCCCCCCOS(=O)(=O)NC(=O)Oc1c(-c2ccccc2)cccc1-c1ccccc1
Reaction #5739
title compound
収率 42.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCCCCCCCCCCCOC(=O)NS(=O)(=O)Cl
Reaction #5741
white solid
収率 101.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
—
Reaction #46027
fatty acid chloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCCCCCCCCCCOC(=O)C=Cc1ccccc1
Reaction #47191
Dodecylcinnamate
収率 87.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(O)C(=O)O.O=C(O)CO
Reaction #50427
GLYCOLIC ACID LACTIC ACID
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
CC(O)C(=O)O.CCCCC(O)C(=O)O
Reaction #50428
lactic acid hydroxycaproic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
C[C@]12CC[C@@H]3c4ccc(OC(=O)c5ccccc5)cc4CC[C@H]3[C@@H]1CC[C@@H]2O
Reaction #51282
Estradiol Benzoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CCCCCCCCCCCCOCCCCCCCCCCCC
Reaction #55334
Dodecyl ether
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
CCCCCCCCCCCCOC(=O)C(Cl)CO
Reaction #67775
dodecyl 2-chloro-3-hydroxypropionate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCCCCCCCCCCCN(C)C
Reaction #191340
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCCCCCCCCCO
Reaction #215164
lauryl alcohol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_03
CCCCCCCCCCCCOc1ccc(C(=O)O)o1
Reaction #239883
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCCCCCCCCCCO
Reaction #258067
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCCCCCCCCCCOC(=O)C=Cc1ccccc1
Reaction #284752
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCCCCCCCCCCCOC(=O)CCl
Reaction #297024
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCCCCCCCCCCCOC(=O)Cc1nc(-c2ccc(Cl)cc2)oc1-c1ccco1
Reaction #323068
lauryl 2-[2-(4-chlorophenyl)-5-(2-furyl)-4-oxazolyl]acetate
収率 77.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_02
CCCCCCCCCCCCOP(=O)(CC(=O)Nc1c(C(C)C)cccc1C(C)C)c1ccccc1
Reaction #335006
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_05
CCCCCCCCCCCCOC(=O)C(C)O
Reaction #336820
lauryl lactate
収率 83.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
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