acrolein

CC(C)n1c(C=CC=O)c(-c2ccc(F)cc2)c2ccccc21
Reaction #10032
3-[3-(4-Fluorophenyl)-1-(1-Methylethyl)-1H-Indol-2-yl]-2-Propenal
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(C)n1c(C=CC=O)c(-c2ccc(F)cc2)c2ccccc21
Reaction #10034
3-[3-(4-Fluorophenyl)-1-(1-Methylethyl)-1H-Indol-2-yl]-2-Propenal
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
c1cnc2c(c1)CCCc1[nH]ncc1-2
Reaction #51706
3,4,5,6-tetrahydro-2,3,10-triaza-benzo[e]azulene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CCOC(=O)C(CCC=O)C(=O)OCC
Reaction #54190
yellow oil
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
CC1=CCC(CO)CC1
Reaction #61886
4-methyl-3-cyclohexenylmethanol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
C=CC(=O)O.C=CC=O
Reaction #66012
acrolein acrylic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
C=CC(=O)O.C=CC=O
Reaction #66013
acrolein acrylic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
C=CC(=O)O.C=CC=O
Reaction #66014
acrolein acrylic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
C=CC=O
Reaction #66015
acrolein
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=COC1CC2CC1C1OC=CCC21
Reaction #78804
3-oxa-tricyclo[6.2.1.02,7]undec-4-ene-10-yl formate
Ausbeute 49.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
COc1ccc2cccnc2c1C(=O)O
Reaction #92484
title compound
Ausbeute 20.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
O=C[C@@H]1CCC=C2CCCO[C@@H]21
Reaction #160824
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(C)(C)OC(=O)COc1cc(C=CC=O)ccc1Cl
Reaction #178581
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
C=CC(O)c1cc(F)cc(F)c1F
Reaction #181259
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=CC(Cl)Cc1ccccc1Cl
Reaction #191503
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)C1=CCCC(C=O)C1
Reaction #192233
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
C=CC(O)C(NC(=O)c1cn(C)nc1C(F)(F)F)C(=O)OCC
Reaction #193080
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1nscc1-c1cn(CCC=O)c(=O)[nH]c1=O
Reaction #200892
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
C=CC(O)c1ccc(Oc2ccccc2)cc1
Reaction #216973
title compound
Ausbeute 73.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11
Cc1ccc(CC2CN(CCC=O)CCN2C(=O)c2cc(C(F)(F)F)cc(C(F)(F)F)c2)cc1C
Reaction #253607
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
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