methyl 6-bromohexanoate

COC(=O)CCCCCOc1ccc(NC(C)=O)cc1
Reaction #170968
15
Ausbeute 42206.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COC(=O)CCCCCOc1ccc([N+](=O)[O-])cc1
Reaction #170975
21
Ausbeute 65.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COC(=O)CCCCCOc1ccc([N+](=O)[O-])c(Nc2ccc(C)cc2)c1
Reaction #189977
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCc1c(OCCCCCC(=O)OC)ccc(C(C)=O)c1O
Reaction #203543
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)CCCCCn1c(-n2ccnc2)c(C)c2ccccc21
Reaction #230851
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COC(=O)CCCCCOc1ccc2cc(C(C)C(=O)OC)ccc2c1
Reaction #270644
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COC(=O)CCCCCN(c1ccc2c(c1)nc(-c1ccccc1)n2-c1ccccc1)S(=O)(=O)c1ccc(F)cc1
Reaction #302077
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COC(=O)CCCCCNC(=O)OC
Reaction #312137
6-methoxycarbonylaminohexanoic acid methyl ester
Ausbeute 77.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_11
COC(=O)CCCCCOc1ccc([N+](=O)[O-])c(Nc2ccccc2)c1
Reaction #380555
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
—
Reaction #410961
ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_04
O=C(O)CCCCCNCC(=O)O
Reaction #449656
6-[(carboxymethyl)amino]hexanoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_02
COC(=O)CCCCCN1CCO[C@H](OCc2cc(C(F)(F)F)cc(C(F)(F)F)c2)[C@H]1c1ccccc1
Reaction #450310
product
Ausbeute 65.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_02
COC(=O)CCCCCn1c2c(c3ccccc31)CN(C)CC2
Reaction #490813
title compound
Ausbeute 41.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_06
COC(=O)CCCCCN(c1ccccn1)c1ccccn1
Reaction #491316
II
Ausbeute 24.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_06
COC(=O)CCCCCOc1ccc([N+](=O)[O-])c(Nc2ccccc2)c1
Reaction #547690
6-(3-Phenylamino-4-nitrophenyl)oxyhexanoic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_03
COC(=O)CCCCCOc1ccc([N+](=O)[O-])c(Nc2ccc(C)cc2)c1
Reaction #547696
6-[3-(4-Methylphenyl)amino-4-nitrophenyl]oxyhexanoic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_03
COC(=O)CCCCCOc1ccc(NC(C)=O)cc1
Reaction #589020
15
Ausbeute 42206.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_08
COC(=O)CCCCCOc1ccc([N+](=O)[O-])cc1
Reaction #589024
21
Ausbeute 65.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_08
COC(=O)CCCCCN(c1ccccn1)c1ccccn1
Reaction #611072
II
Ausbeute 24.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
COC(=O)CCCCCN1CCO[C@H](OCc2cc(C(F)(F)F)cc(C(F)(F)F)c2)[C@H]1c1ccccc1
Reaction #669286
product
Ausbeute 65.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_07
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