octanal

O=Cc1ccccc1
Reaction #2498
benzaldehyde
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCCCC(C=O)=Cc1ccccc1
Reaction #2499
α-hexylcinnamaldehyde
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCCCC(C=O)=Cc1ccccc1
Reaction #2500
α-hexylcinnamaldehyde
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
C=C(C=O)CCCCCC
Reaction #43900
a-methylene octanal
Ausbeute 1636.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCCCCCC=C(C(=O)OCC)C(=O)c1ccccc1
Reaction #92783
2-benzoyl-dec-2-enoic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CCCCCCCC=CCCCCCO
Reaction #199231
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCCCCC=C1CCCC1=O
Reaction #205828
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCCCCC(O)c1ccc(C=COC)cc1
Reaction #215978
1-(4-(2-methoxyethenyl)phenyl)-1-octanol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11
CCCCCCCC=O
Reaction #262120
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCCCCCCC=O
Reaction #301806
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCCCCCCC(=O)O
Reaction #398294
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCCCCCCC=C1SC(=O)N(CCCCSc2cccc3nccn23)C1=O
Reaction #444354
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_11
CCCCCCCC1N[C@@H](C(=O)O)Cc2c1[nH]c1ccccc21
Reaction #448742
(3R)-1,2,3,4-Tetrahydro-1-heptyl-β-carboline-3-carboxylic Acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_02
CCCCCCCC=O
Reaction #460933
n-Octanal
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1992_11
CCCCCCCC(O)CC(=O)OC
Reaction #482092
Methyl 3-hydroxydecanoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_08
CCCCCCCC(O)CC(=O)O
Reaction #483086
3-Hydroxydecanoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_08
CCCCCCCC(O)C(C)C(=O)OC
Reaction #483087
Methyl 3-hydroxy-2-methyldecanoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_08
CCCCCCCC=O
Reaction #486790
octanal
Ausbeute 91.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_10
CCCCCCCC=O
Reaction #544640
white solid
Ausbeute 234.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_03
CCCCCCCC=NO
Reaction #544641
pale yellow solid
Ausbeute 270.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_03
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