stearic acid

CCCCCCCCCCCCCCCCCCN(C)CCOC(=O)CCCCCCCCCCCCCCCCC
Reaction #2057
N-(2-octadecanoyloxyethyl)-N-methyloctadecylamine
수율 96.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C=O)=CCC1CC=C(C)C1(C)C
Reaction #43897
2-methyl-4-(2,2,3-trimethylcyclopent-3-en-1-yl)-but-2-en-1-al
수율 94.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
C=C(C=O)CCCCCCCCC
Reaction #43899
α-methylene undecanal
수율 1583.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCCCCCCCCCCCCCCCC(=O)[O-].[Ag+]
Reaction #44319
silver stearate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCCCCCCCCCCCCCCCC(=O)[O-].CCCCCCCCCCCCCCCCCC(=O)[O-].[Cu+2]
Reaction #44320
copper stearate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCCCCCCCCCCCCCCC(Cl)C(=O)O
Reaction #54448
2-chlorostearic acid
수율 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
CCCCCCCCCCCCCCCCCC(=O)[O-].CCCCCCCCCCCCCCCCCC(=O)[O-].[Zn+2]
Reaction #55314
zinc stearate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
CCCCCCCCCCCCCCCCCC(=O)O.OCCN(CCO)CCO
Reaction #71259
Triethanolamine Stearate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCCCCCCCCCCCCCCCCC(=O)OCC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)C
Reaction #75234
3,7,11,15,19,23,27,31,35-Nonamethyl-2,6,10,14,18,22,26,30,34-hexatriacontanonaenyl stearate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_11
CCCCCCCCCCCCCCCCCCCCCC(=O)[O-].[Na+]
Reaction #75460
sodium behenate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
—
Reaction #82997
polyunsaturated fatty acid
수율 26.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
—
Reaction #82998
polyunsaturated fatty acid
수율 8.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
C=C(C)C(=O)OCC1CO1
Reaction #94105
glycidyl methacrylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_12
CCCCCCCCCCCCCCCCCCN(C)CCOC(=O)CCCCCCCCCCCCCCCCC
Reaction #175072
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCCCCCCCCCCCCCCCCl
Reaction #177410
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCCCCCCCCCCCCCCC(=O)Cl
Reaction #253944
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCCCCCCCCCCCCCCCC(=O)Cl
Reaction #264713
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCCCCCCCCCCCCCCCCC(=O)NCCCCCC(=O)N1CC(O)CC1C(OCc1ccc(OC)cc1)(c1ccccc1)c1ccc(OC)cc1
Reaction #265768
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCCCCCCCCCCCCCCCCC(=O)CC(=O)OC
Reaction #271028
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCCCCCCCCCCCCCCCCC(=O)Cl
Reaction #304726
white solid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
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