n-hexyl amine

CCCCCCN.O=C1CCCCCN1
Reaction #56355
Caprolactam n-Hexylamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
CCCCCCNc1ccc([N+](=O)[O-])cc1F
Reaction #84455
title compound
収率 91.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CCCCCCN(CCC#N)CCC#N
Reaction #161892
target compound
収率 98.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCCCCCNCc1ccccc1C#Cc1ccc(CCCC)cc1
Reaction #174605
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCCCNC1=C(c2ccccc2)S(=O)(=O)N(CCCC)C1=O
Reaction #182387
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCCCNc1ccccc1CO
Reaction #183395
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCCCNc1nc2ccccc2n1C1CCN(C(=O)c2ccc(CCCC)cc2)CC1
Reaction #186781
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCCCNc1ccc(Br)cc1
Reaction #210078
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCCCNCc1ccc(F)c(C(=O)OC)c1
Reaction #211240
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCCCNC(=O)C12CCC(N(CC(=O)N3CC(F)CC3C#N)C(=O)OCc3ccccc3)(CC1)CC2
Reaction #212724
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCCCNCc1ccc(Oc2ccc(C(N)=O)cn2)c(OC)c1
Reaction #218050
title compound
収率 73.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
CCCCCCNCc1ccc(Oc2cnc(C(N)=O)cn2)c(F)c1
Reaction #218181
title compound
収率 62.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
CCCCCCNC(=O)c1ccc2c(c1)nc(COc1ccccc1)n2Cc1ccc(OC(F)(F)F)cc1
Reaction #218402
2-Phenoxymethyl-1-(4-trifluoromethoxy-benzyl)-1H-benzoimidazole-5-carboxylic acid hexylamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
CCCCCCNc1ccc(C#N)cc1
Reaction #226115
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCCCCNc1cc(C#N)ccn1
Reaction #226671
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCCCCNC(=O)C=CC(=O)O
Reaction #227169
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCCCCNc1nsnc1-c1cccnc1
Reaction #228542
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCCCCNCc1ccccc1
Reaction #245348
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCCCCNc1nc(Cl)nc2c1ncn2C1CCCC1
Reaction #245498
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCCCCNC(=O)c1ccc(NC(=O)CCC(=O)O)cc1O
Reaction #246765
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
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