1-(2-chloroethyl)-piperidine

N#CC(CCN1CCCCC1)c1ccccc1Cl
Reaction #3052
(±)-α-(2-chlorophenyl)-1-piperidinebutanenitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
—
Reaction #3054
( b )
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CS(=O)(=O)Nc1ccc(NS(C)(=O)=O)c(SCCN2CCCCC2)c1.Cl
Reaction #54200
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
CCN(CCc1ccc(OCCN2CCCCC2)cc1)c1cc(OC)ccc1C1CCc2cc(OC)ccc2C1
Reaction #178893
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
NC(=O)c1ccc(-c2cn(CCN3CCCCC3)nc2OCc2ccccc2)cc1
Reaction #182528
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=[N+]([O-])c1ccc2nn(CCN3CCCCC3)cc2c1
Reaction #189748
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1nc(NC(=O)N(C2CCCCC2)C2CCCCC2)sc1SCCN1CCCCC1
Reaction #191937
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
NC(=O)Nc1cc(-c2cccc(OCCN3CCCCC3)c2)sc1C(N)=O
Reaction #198003
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
NN(CCN1CCCCC1)c1ccc(Cl)cc1
Reaction #207579
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)c1cc2cccc(OCc3ccccc3)c2cc1OCCN1CCCCC1
Reaction #209281
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc(-c2sc3cc(OC)ccc3c2C(=O)c2ccc(OCCN3CCCCC3)c(C#N)c2)cc1
Reaction #213257
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc(C(c2ccc(OCCN3CCCCC3)cc2)c2cccc3ccccc23)cc1
Reaction #213739
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C1c2ccccc2S(=O)(=O)N1CSc1nnc(SCCN2CCCCC2)s1
Reaction #226656
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)N(CCC(C#N)(CCN1CCCCC1)c1ccccn1)C(C)C
Reaction #227496
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
C1=CC(Oc2nn(CCN3CCCCC3)cc2-c2ccccn2)CCC1
Reaction #228283
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCOC(=O)c1ccc(OCCN2CCCCC2)cc1
Reaction #232344
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Clc1ccc(-c2cn(CCN3CCCCC3)nc2OCc2ccccc2)cc1Cl
Reaction #238755
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=[N+]([O-])c1cccc2nn(CCN3CCCCC3)cc12
Reaction #242647
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
c1ccc(OCCSCc2nnc(-c3ccc(OCCN4CCCCC4)cc3)o2)cc1
Reaction #250541
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cl
Reaction #254553
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
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