hexanal

CCCCc1c[nH]c2ccc(C(=O)OCC)cc12
Reaction #42489
title compound
المردود 7.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCCc1cnc2ccc(C(=O)O)cn12
Reaction #42514
3-butylimidazo[1,2-a]pyridine-6-carboxylic acid
المردود 11.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCCCC(CCN)OC1CCCCO1
Reaction #56479
title compound
المردود 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
CCCCCC1OC(C)(C)C=CC(C)(C)O1
Reaction #62708
2-pentyl-4,4,7,7-tetramethyl-4,7-dihydro-1,3-dioxepin
المردود 70.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
CCCCCCN[C@@H]1CN(c2nc3cccc(C(=O)OCC)c3s2)CC[C@@H]1NC(=O)c1nc(Cl)c(CC)[nH]1
Reaction #71824
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCCCCC=O.OCC(O)CO
Reaction #161313
n-Hexanal Glycerol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCCCCC=NC(C)(C)C
Reaction #163426
N-(tert-butyl)-N-hexylideneamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCCCc1cn(C(C)(C)C)s/c1=N\C(=O)OCC
Reaction #163456
title compound
المردود 92.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCCCc1cn(C(C)(C)C(F)(F)F)s/c1=N\C(=O)OCC
Reaction #163486
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCCCCC=NC(C)(C)CF
Reaction #163487
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCCCCCN(Cc1ccc(C#Cc2ccc(CCCC)cc2)cc1)c1ccc(F)c(C(=O)OC)c1
Reaction #192930
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCCC(C#C[Si](C)(C)C)N1CCC(=O)CC1
Reaction #197508
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCCCN1CCCC(c2ccc(Oc3ccc(C(N)=O)cn3)cc2)C1
Reaction #217931
title compound
المردود 30.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
CCCCCCN(Cc1ccc(C#Cc2ccccc2)cc1)c1ccc(F)c(C(=O)OC)c1
Reaction #223561
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCCCCN(Cc1ccc(C#Cc2ccc(CC)cc2)cc1)c1ccc(F)c(C(=O)OC)c1
Reaction #223919
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCCCCN(Cc1ccc(C#Cc2ccc(C(C)(C)C)cc2)cc1)c1ccc(F)c(C(=O)OC)c1
Reaction #252921
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCCCCN(C(=O)Nc1ncc(SCC(=O)O)s1)c1cccc(NC(C)=O)c1
Reaction #263485
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCCCCC=CC#N
Reaction #268798
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCCCCC1OCc2cc(C(=O)O)ccc2O1
Reaction #289643
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCCc1ccc(CCCCC(C(=O)OCC)C(=O)OCC)cc1
Reaction #293833
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
الصفحة 1التالي