An 312 Reaktionen beteiligt

CCCCCCCCCCCCN

CCCCCCCCCCCCNCCCSc1ccncc1

desired compound

Ausbeute 29.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09

CCCCCCCCCCCCNC(N)=O

DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09

CCCCCCCCCCCCN

Ausbeute 83.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08

CCCCCCCCCCCCNc1cc(C)nc(C(C)C)n1

Reaction #42624

4-dodecylamino-2-isopropyl-6-methylpyrimidine

DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06

CCCCCCCCCCCCNC(=O)NS(=O)(=O)CCCl

Reaction #54630

N-lauryl-N'-β-chlorethylsulphonyl urea

DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04

CCCCCCCCCCCCNC(=O)c1ccc(C(=O)OC)cc1

Reaction #175989

DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)

CCCCCCCCCCCCN1CCCC1C(=O)OCC

Reaction #179815

DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)

CCCCCCCCCCCCNC(=O)Nc1c(C)ccc2c1OCCC2=O

Reaction #183345

DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)

CCCCCCCCCCCCNC(=O)c1ccc(C(C)=O)cc1

Reaction #185858

DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)

CCCCCCCCCCCCNCC#N

Reaction #188074

DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)

CCCCCCCCCCCCN(C)C

Reaction #191340

DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)

CCCCCCCCCCCCNCCCOc1ccc2ccccc2c1

Reaction #197143

DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)

CCCCCCCCCCCCNC(=O)c1cc(C(O)CN2CCN(c3ccccc3C)CC2)ccc1O.Cl

Reaction #214657

N-dodecyl-2-hydroxy-5-[1-hydroxy-2-[4-(2-methylphenyl)-1-piperazinyl]ethyl]benzamide hydrochloride

DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_03

CCCCCCCCCCCCNCC(O)CO

Reaction #216078

3-Laurylamino-1,2-Dihydroxy-Propane

Ausbeute 59.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11

CCCCCCCCCCCCc1ccc[nH]c1=O

Reaction #217447

Dodecyl Pyridone

Ausbeute 85.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06

CCCCCCCCCCCCNC(N)=O

Reaction #228916

DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)

CCCCCCCCCCCCNS(=O)(=O)c1ccc(CN2C(=O)c3ccccc3C2=O)s1

Reaction #230704

DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)

CCCCCCCCCCCCNCCCCOc1ccc2ccccc2c1

Reaction #235991

DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)

CCCCCCCCCCCCNC(=O)COc1ccc(C=CC(=O)C(F)(F)F)cc1

Reaction #238151

DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)

O=C(O)C=CC(=O)O

Reaction #240841

DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)

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