cinnamaldehyde

O=CC=Cc1ccccc1.O=Cc1ccccc1
Reaction #4578
Benzaldehyde Cinnamaldehyde
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
O=CC=Cc1ccccc1.O=Cc1ccccc1
Reaction #4596
BENZALDEHYDE CINNAMALDEHYDE
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
O=CC=Cc1ccccc1.O=Cc1ccccc1
Reaction #4865
Benzaldehyde Cinnamaldehyde
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
O=C1C(c2ccccc2)=C(c2ccccc2)CCC1c1ccccc1
Reaction #5147
2,3,6-triphenylcyclohexenone
Ausbeute 91.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
C1=NNC(c2ccccc2)C1
Reaction #40773
5-Phenyl-4,5-dihydro-1H-pyrazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COC(=O)C=Cc1ccccc1
Reaction #47180
Methyl cinnamate
Ausbeute 98.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)OC(=O)C=Cc1ccccc1
Reaction #47182
Isopropyl cinnamate
Ausbeute 49.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C(C=Cc1ccccc1)OCCCc1ccccc1
Reaction #47183
3-Phenylpropyl cinnamate
Ausbeute 84.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COC(=O)C=Cc1ccccc1
Reaction #47186
Methyl cinnamate
Ausbeute 98.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COC(=O)C=Cc1ccccc1
Reaction #47187
Methyl cinnamate
Ausbeute 96.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCOC(=O)C=Cc1ccccc1
Reaction #47188
Ethyl cinnamate
Ausbeute 94.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCCOC(=O)C=Cc1ccccc1
Reaction #47189
Butyl cinnamate
Ausbeute 94.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCCCCCCOC(=O)C=Cc1ccccc1
Reaction #47190
Octyl cinnamate
Ausbeute 86.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCCCCCCCCCCOC(=O)C=Cc1ccccc1
Reaction #47191
Dodecylcinnamate
Ausbeute 87.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COCCOC(=O)C=Cc1ccccc1
Reaction #47192
2-Methoxyethyl cinnamate
Ausbeute 93.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C(C=Cc1ccccc1)OCCO
Reaction #47193
2-Hydroxyethyl cinnamate
Ausbeute 88.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C(O)CCC=Cc1ccccc1
Reaction #64694
5-phenyl-4-pentenoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
C=CCOC(C(=O)OCC)C(O)C=Cc1ccccc1
Reaction #188398
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(C=Cc1ccccc1)N(O)c1ccccc1
Reaction #189641
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(=O)C(=CC=Cc1ccccc1)c1ccncc1
Reaction #245859
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
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