#NOCCO

CC1(C)c2cc(C(=O)NOCCO)ccc2C(=O)c2c1[nH]c1cc(C#N)ccc21
Reaction #90047
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
O=C(NOCCO)c1ccc(F)c(F)c1Nc1ccc(C#CCOC2CCCCO2)cc1F
Reaction #183434
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cn1cc(C(=O)NOCCO)c(Nc2ccc(Br)cc2F)cc1=O
Reaction #222572
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cn1cc(C(=O)NOCCO)c(Nc2ccc(I)cc2F)cc1=O
Reaction #248397
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(=NOCCO)c1ccc2nnc(C(C)c3c(F)cc4ncccc4c3F)n2n1
Reaction #259328
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(NOCCO)c1ccc(F)c(F)c1Nc1ccc(C#CCCOC2CCCCO2)cc1F
Reaction #273309
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCCCc1ccc(Nc2c(C(=O)NOCCO)ccc(F)c2F)c(F)c1
Reaction #282080
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC(=NOCCO)c1ccc2ncc(C(C)c3c(F)cc4c(cnn4C)c3F)n2n1
Reaction #296439
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC(=NOCCO)c1cnc2nnn(C(C)c3c(F)cc4ncccc4c3F)c2n1
Reaction #299497
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COC(=O)c1ccc(Nc2c(C(=O)NOCCO)ccc(F)c2F)c(F)c1
Reaction #300886
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COC(=O)c1ccc(Nc2c(C(=O)NOCCO)ccc(F)c2F)cc1
Reaction #381563
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
O=C(NOCCO)c1ccc(F)c(F)c1Nc1ccc(CCO)cc1F
Reaction #404647
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
Nc1c(Cl)cc(Cl)cc1C(=O)NOCCO
Reaction #536977
3,5-dichloro-2-amino-N-(2-hydroxyethoxy)benzamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
Nc1c(Cl)cc(Cl)cc1C(=O)NOCCO
Reaction #645249
3,5-dichloro-2-amino-N-(2-hydroxyethoxy)benzamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_11
Cc1ccc(Nc2cc(=O)n(C)cc2C(=O)NOCCO)c(F)c1
Reaction #749961
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
CC(=NOCCO)c1ccc2ncc(Cc3c(F)cc4c(cnn4C)c3F)n2n1
Reaction #766833
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
CC(=NOCCO)c1ccc2ncc(C(C)c3cc4cnn(C)c4cc3F)n2n1
Reaction #769174
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
CC(=NOCCO)c1cnc2nnn(Cc3ccc4ncccc4c3)c2n1
Reaction #780991
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
Nc1c(Cl)cc(Cl)cc1C(=O)NOCCO
Reaction #898744
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
CNC(=O)c1ccc(Nc2c(C(=O)NOCCO)ccc(F)c2F)c(F)c1
Reaction #920120
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
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