6-(4-amino-phenoxy)hexanoic acid methyl ester

COC(=O)CCCCCOc1ccc(N=C=O)cc1
Reaction #170972
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Ausbeute 72.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COC(=O)CCCCCOc1ccc(NC(=O)COCc2ccccc2)cc1
Reaction #170999
53
Ausbeute 22.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COC(=O)CCCCCOc1ccc(N=C=O)cc1
Reaction #589022
18
Ausbeute 72.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_08
COC(=O)CCCCCOc1ccc(NC(=O)COCc2ccccc2)cc1
Reaction #589047
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Ausbeute 22.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_08
COC(=O)CCCCCOc1ccc(N=C=O)cc1
Reaction #725907
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Ausbeute 72.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_04
COC(=O)CCCCCOc1ccc(NC(=O)COCc2ccccc2)cc1
Reaction #725933
70
Ausbeute 22.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_04
COC(=O)CCCCCOc1ccc(N=C=O)cc1
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18
Ausbeute 72.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_03
COC(=O)CCCCCOc1ccc(NC(=O)COCc2ccccc2)cc1
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53
Ausbeute 22.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_03
COC(=O)CCCCCOc1ccc(N=C=O)cc1
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Ausbeute 72.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_04
COC(=O)CCCCCOc1ccc(NC(=O)COCc2ccccc2)cc1
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Ausbeute 22.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_04
COC(=O)CCCCCOc1ccc(NC(=O)COCc2ccccc2)cc1
Reaction #2241443
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (4/10)
COC(=O)CCCCCOc1ccc(NC(=O)COCc2ccccc2)cc1
Reaction #2244296
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (4/10)
COC(=O)CCCCCOc1ccc(N=C=O)cc1
Reaction #2256902
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Ausbeute 72.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_06
COC(=O)CCCCCOc1ccc(NC(=O)COCc2ccccc2)cc1
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Ausbeute 22.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_06