octan-1-amine

CCCCCCCCNc1nc(NCCCCCCCC)nc(Nc2ccc(OCC(COc3ccc(Nc4nc(NCCCCCCCC)nc(NCCCCCCCC)n4)cc3)(COc3ccc(Nc4nc(NCCCCCCCC)nc(NCCCCCCCC)n4)cc3)COc3ccc(Nc4nc(NCCCCCCCC)nc(NCCCCCCCC)n4)cc3)cc2)n1
Reaction #8512
1,3-bis(4-[N-(2,4-bis(N-octylamino)-1,3,5-triazin-6-yl)amino]phenoxy)-2,2-bis [(4-[N-(2,4-bis(N-octylamino)—1,3,5-triazin-6-yl)amino]phenoxy)methyl]propane
収率 69.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCCCCCCCNc1nc(NCCCCCCCC)nc(Nc2ccc(OCCCCCOc3ccc(Nc4nc(NCCCCCCCC)nc(NCCCCCCCC)n4)cc3)cc2)n1
Reaction #8514
1,5-Bis[4-[N-[4,6-bis(N-octylamino)-1,3,5-triazin-2-yl]amino]phenoxy]pentane
収率 45.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCCCCCCCNCCCOc1ccc(SC)cc1
Reaction #54283
N-[3-[4-(methylthio)phenoxy]propyl]octylamine
収率 22.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
CCCCCCCCNCCOc1ccc(SC(C)C)cc1.Cl
Reaction #54288
N-[2-[4-[(1-methylethyl)thio]phenoxy]ethyl]octylamine hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
CCCCCCCCNC(=O)CCS
Reaction #65732
N-(n-octyl)-3-mercaptopropionamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
CCCCCCCCNCCC(=O)O
Reaction #93698
N-n-octyl-β-alanine
収率 78.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_09
CCCCCCCCNC(=O)C=Cc1ccccc1[N+](=O)[O-]
Reaction #95087
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
CCCCCCCCNC(=O)[C@@H]1C[C@H]1c1ccc([N+](=O)[O-])cc1
Reaction #95092
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
CCCCCCCCNS(=O)(=O)CC1=CC(C)(C)N(CC)c2ccccc21
Reaction #171326
(1-Ethyl-2,2-dimethyl-1,2-dihydroquinol-4-yl)-N-octyl-methanesulfonamide
収率 81.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCCCCCCCNS(=O)(=O)CC1CC(C)(C)N(C)c2cc(OC)ccc21
Reaction #171329
(1-Methyl-7-methoxy-2,2-dimethyl-1,2,3,4-tetrahydroquinol-4-yl)-N-octyl-methane-sulfonamide
収率 69.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
C#CC(=O)NCCCCCCCC
Reaction #174923
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCCCCCNCCCOc1ccc(SC)cc1
Reaction #176862
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCCCCCNC(=O)C1CCCN(C(=O)c2ccccc2)C1
Reaction #180588
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCCCCCNC(=O)C12CCC(N(CC(=O)N3CC(F)CC3C#N)C(=O)OCc3ccccc3)(CC1)CC2
Reaction #185640
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCCCCCNC(=O)C1CCCCCN1C(=O)OC(C)(C)C
Reaction #192852
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCCCCCN1CCN(CCO)C1=O
Reaction #202787
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCCCCCNC(=O)CCCCCC
Reaction #215478
N-octylhexanecarboxamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_03
CCCCCCCCNS(=O)(=O)c1ccc(C(=O)O)cc1
Reaction #215982
4-(Octylaminosulfonyl)benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11
CCCCCCCCN=CN(C)C
Reaction #222986
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCCCCCCNc1nc(C(=O)OCC)cs1
Reaction #246143
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
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