2-amino-1-hexanol

CCCCC(CO)NC(=O)C(CC(C)C)NC(=O)OCc1ccccc1
Reaction #231313
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCCC(CO)NC(=S)NC(C)(C)C
Reaction #241932
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCCC(CO)Nc1cc2c(=O)n(NS(C)(=O)=O)c(=O)[nH]c2cc1[N+](=O)[O-]
Reaction #292156
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCCCC(N)COC(=O)CCSSCCC(=O)OCC(N)CCCC
Reaction #1340584
di(2-aminohexyl) 3,3′-dithiodipropionate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_06
CCCCC(CO)Nc1ccc([N+](=O)[O-])cc1C(=O)NCc1ccc2c(c1)OCO2
Reaction #1633498
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (1/10)
CCCCC1COC(=S)N1
Reaction #1808467
4-butyloxazolidine-2-thione
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_04
CCCCC1COC(=S)N1
Reaction #1816449
4-butyloxazolidine-2-thione
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1994_07
CCCCC(CO)Nc1nc(SCc2ccccc2)nc2nc(N)sc12
Reaction #1918644
title compound
Ausbeute 17.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_06
CCCCC(CO)Nc1nc(SCc2cccc(F)c2F)nc2nc(N)sc12
Reaction #1918652
(±)-2-[2-Amino-5-(2,3-difluorophenylmethylthio)-thiazolo[4,5-d]pyrimidin-7-ylamino]-hexan-1-ol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_06
CCCCC(CO)Nc1ccc([N+](=O)[O-])cc1C(=O)NCc1ccc2c(c1)OCO2
Reaction #2021839
2-[1-(1-Hydroxymethyl)pentylamino]-5-nitro-N-(1,3-benzodioxol-5-ylmethyl)benzamide
Ausbeute 77.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_05
CCCCC(CO)Nc1cc2c(=O)n(NS(C)(=O)=O)c(=O)[nH]c2cc1[N+](=O)[O-]
Reaction #2156429
purple powder
Ausbeute 61.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_10
CCCCC(N)COCC1CCN(C(=O)OC(C)(C)C)CC1
Reaction #2437257
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (10/10)