#4524226

CC(=O)[n+]1c(C2CCCCC2)c(NC2CCCCC2)n2ccccc21.[Cl-]
Reaction #7625
1-acetyl-2-cyclohexyl-3-cyclohexylamino-imidazo[1,2-a]pyridin-1-ium chloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC1CC(=CC2CCCCC2)C(=O)O1
Reaction #65055
3-cyclohexylmethylene-5-methyldihydro-2(3H)-furanone
收率 97.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
Cc1cc(C2CCCCC2)c(C#N)c(=O)[nH]1
Reaction #70735
4-cyclohexyl-6-methyl-2-oxo-1,2-dihydro-3-pyridinecarbonitrile
收率 32.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCOC(CNCC1CCCCC1)OCC
Reaction #71532
N-cyclohexylmethyl-(2,2-diethoxyethyl)amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
C1CCC(C2CO2)CC1
Reaction #82415
1-cyclohexyl ethylene oxide
收率 62.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
Cc1cc(C2CCCCC2)c(C#N)c(=O)[nH]1
Reaction #90634
4-cyclohexyl-6-methyl-2-oxo-1,2-dihydro-3-pyridinecarbonitrile
收率 32.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
O=C(C=CC1CCCCC1)CCCCCl
Reaction #96164
1-cyclohexyl-7-chloro-1-hepten-3-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
Cl.Cl.Cn1c(=O)c(OCCCCCN(CCc2cccnc2)CC2CCCCC2)cc2ccccc21
Reaction #156185
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1cc(C2CCCCC2)c(C#N)c(=O)[nH]1
Reaction #172714
4-cyclohexyl-6-methyl-2-oxo-1,2-dihydro-3-pyridinecarbonitrile
收率 32.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
NS(=O)(=O)c1ccc2c(c1)S(=O)(=O)NC(C1CCCCC1)N2
Reaction #183637
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COCCCN1CCOc2ccc(COC3CN(C(=O)OCc4ccccc4)CCC3c3ccc(OCCNCC4CCCCC4)cc3)cc21
Reaction #196046
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(Nc1ccc(OC(F)(F)F)cc1)Nc1cccnc1Oc1cccc2c1CCN(CC1CCCCC1)C2
Reaction #196106
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)Cc1c(Cl)nc(Cc2ccc(NCC3CCCCC3)cc2)nc1N(C)CC(=O)NC1CCCC1
Reaction #197748
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
FC(F)(F)c1nnc2ccc(N3CCN(CC4CCCCC4)CC3)nn12
Reaction #197874
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
C[Si](C)(C)CCOCn1ccc2c(-n3cc(C(O)C4CCCCC4)cn3)ccnc21
Reaction #198900
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
C=CC(O)C1CCCCC1
Reaction #203451
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
N#CCCC1(C=O)CCCCC1
Reaction #204765
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C1Nc2ccc(Cl)cc2C1=CC1CCCCC1
Reaction #207690
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)C(c1ccccc1OCc1ccccc1)C(O)C1CCCCC1
Reaction #212878
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
NC(=O)c1ccc(Oc2ccc(C3CCCN(CC4CCCCC4)C3)cc2)nc1
Reaction #217928
title compound
收率 19.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
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