5,6-dinitrobenzo[d][1,3]dioxole

O=[N+]([O-])c1cc2c(cc1NCC(O)CO)OCO2
Reaction #269995
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=[N+]([O-])c1cc(O)c(OCCOCCO)cc1[N+](=O)[O-]
Reaction #375742
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CNc1cc2c(cc1[N+](=O)[O-])OCO2
Reaction #408663
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
Nc1cc2c(cc1[N+](=O)[O-])OCO2
Reaction #664794
6-nitrobenzo[d][1,3]dioxol-5-amine
Ausbeute 84.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_05
CNc1cc2c(cc1[N+](=O)[O-])OCO2
Reaction #666870
2-methylamino-4,5-methylenedioxy-1-nitrobenzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_06
CCCCNc1cc2c(cc1[N+](=O)[O-])OCO2
Reaction #666871
2-n-butylamino-4,5-methylenedioxy-1-nitrobenzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_06
O=[N+]([O-])c1cc2c(cc1NCC(O)CO)OCO2
Reaction #666872
expected product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_06
COc1cc([N+](=O)[O-])c([N+](=O)[O-])cc1O
Reaction #736833
expected product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_04
O=[N+]([O-])c1cc(O)c(OCCO)cc1[N+](=O)[O-]
Reaction #736834
4,5-dinitro-2-(β-hydroxyethoxy)phenol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_04
O=[N+]([O-])c1cc(O)c(OCCOCCO)cc1[N+](=O)[O-]
Reaction #736835
4,5-dinitro-2-[β-(2-hydroxyethoxy)ethoxy]phenol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_04
COCCOc1cc([N+](=O)[O-])c([N+](=O)[O-])cc1O
Reaction #736836
4,5-dinitro-2-(β-methoxyethoxy)phenol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_04
Nc1cc2c(cc1[N+](=O)[O-])OCO2
Reaction #902734
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
CNc1cc2c(cc1[N+](=O)[O-])OCO2
Reaction #1287051
2-methylamino-4,5-methylenedioxy-1-nitrobenzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1990_02
CCCCNc1cc2c(cc1[N+](=O)[O-])OCO2
Reaction #1287052
2-n-butylamino-4,5-methylenedioxy-1-nitrobenzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1990_02
O=[N+]([O-])c1cc2c(cc1NCC(O)CO)OCO2
Reaction #1287053
expected product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1990_02
Nc1cc2c(cc1[N+](=O)[O-])OCO2
Reaction #1563906
6-nitrobenzo[d][1,3]dioxol-5-amine
Ausbeute 84.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_08
O=[N+]([O-])c1cc(O)c(OCCO)cc1[N+](=O)[O-]
Reaction #1627604
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (1/10)
O=[N+]([O-])c1cc(O)c(OCCOCCO)cc1[N+](=O)[O-]
Reaction #1632633
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (1/10)
COc1cc([N+](=O)[O-])c([N+](=O)[O-])cc1O
Reaction #1653369
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (1/10)
Nc1cc2c(cc1[N+](=O)[O-])OCO2
Reaction #2130075
6-nitrobenzo[d][1,3]dioxol-5-amine
Ausbeute 84.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_11
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