An 415 Reaktionen beteiligt

CCCCCCBr

CCCCCCC(C(C)=O)C(=O)OC
Reaction #5715
methyl 2-acetyloctanoate
Ausbeute 62.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCCCCCC(C(=O)OC)C(=O)OC
Reaction #5719
dimethyl n-hexylmalonate
Ausbeute 78.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCCCCCC1c2ccccc2-c2ccccc21
Reaction #11837
compound 2
Ausbeute 76.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCCCCCN1CCc2nc(NC(=N)N)sc2C1
Reaction #40340
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCCCCOC1CCCCCCCCCCC1
Reaction #64747
n-Hexyloxycyclododecane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
CCCCCCSC(=S)N1Cc2[nH]c3ccccc3c2C[C@H]1CO
Reaction #93345
title compound
Ausbeute 73.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_09
CCCCCCN(C(C)=O)c1ccc(N)cc1
Reaction #173684
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCCCN1CCc2nc(NC(=N)N)sc2C1
Reaction #175857
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCCCc1cccs1
Reaction #177606
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCCCOc1ccc(Br)cc1F
Reaction #180709
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCCCOc1cc2c(cc1C(C)=O)C(C)(C)CCC2(C)C
Reaction #186465
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
C=CCCC(O)CCCCCC
Reaction #196400
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCCCOc1ccc(C#N)cc1OC
Reaction #199102
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCCCSc1nnc(N)s1
Reaction #209619
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCCCn1ccc2c(C=O)cccc21
Reaction #212674
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCCCOc1ccc2cc(Br)ccc2c1
Reaction #216968
title compound
Ausbeute 81.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11
CCCCCCN1CCCc2cc(Oc3ccc(C(N)=O)cn3)ccc2C1
Reaction #218099
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
CCCCCCC1(C(=O)OCC)CCCC1=O
Reaction #219951
Ethyl 1-n-hexyl-2-oxocyclopentane carboxylate
Ausbeute 87.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
CCCCCCOc1ccc(C=O)c(O)c1
Reaction #222238
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCCCCOc1cccc(C(N)=O)c1F
Reaction #229996
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
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