2-nitrobenzylalcohol

O=Cc1ccccc1[N+](=O)[O-]
Reaction #283201
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Cc1ccc(S(=O)(=O)OCc2ccccc2[N+](=O)[O-])cc1
Reaction #298444
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Cc1ccc(S(=O)(=O)OCc2ccccc2[N+](=O)[O-])cc1
Reaction #357718
22
Ausbeute 79.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_11
CCCCCCCCCCCCCCCCS(=O)(=O)OCc1ccccc1[N+](=O)[O-]
Reaction #398276
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
COCc1ccccc1[N+](=O)[O-]
Reaction #426186
1-(methoxymethyl)-2-nitrobenzene
Ausbeute 91.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
CCCCCCCCNC(=O)OCc1ccccc1[N+](=O)[O-]
Reaction #430450
o-nitrobenzyl n-octylcarbamate
Ausbeute 62.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_01
O=C(NC1CCCCC1)OCc1ccccc1[N+](=O)[O-]
Reaction #470382
[[(2-nitrobenzyl)oxy]carbonyl]cyclohexylamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
O=C(NCc1ccccc1)OCc1ccccc1[N+](=O)[O-]
Reaction #486554
o-nitrobenzyl benzylcarbamate
Ausbeute 67.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_10
CCCCCCCCNC(=O)OCc1ccccc1[N+](=O)[O-]
Reaction #529780
ortho-nitrobenzyl n-octylcarbamate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_04
O=C(NC1CCCCC1)OCc1ccccc1[N+](=O)[O-]
Reaction #529781
ortho-nitrobenzyl cyclohexylcarbamate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_04
CCOC(=O)COCc1ccccc1[N+](=O)[O-]
Reaction #564042
ethyl (o-nitro-benzyloxy)acetate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1989_12
CCCCCCCCNC(=O)OCc1ccccc1[N+](=O)[O-]
Reaction #568879
ortho-nitrobenzyl n-octylcarbamate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_08
O=C(NC1CCCCC1)OCc1ccccc1[N+](=O)[O-]
Reaction #568880
ortho-nitrobenzyl cyclohexylcarbamate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_08
C=C(C)C(=O)OCCNC(=O)OCc1ccccc1[N+](=O)[O-]
Reaction #679305
2-({[(2-nitrobenzyl)oxy]carbonyl}amino)ethyl 2-methylacrylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_01
O=C(OCc1ccccc1[N+](=O)[O-])C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F
Reaction #736885
2-Nitrobenzyl perfluorooctanoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_04
CCCCCCCCCCCCCCCCCC(=O)OCc1ccccc1[N+](=O)[O-]
Reaction #736887
2-Nitrobenzyl octadecanoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_04
CCCCCCCCCCCCCCCCS(=O)(=O)OCc1ccccc1[N+](=O)[O-]
Reaction #736888
2-Nitrobenzyl hexadecanesulfonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_04
O=C(CCCCCCCCCCS)OCc1ccccc1[N+](=O)[O-]
Reaction #744645
2-nitrobenzyl 11-mercaptoundecanoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_12
C=CCCCCCCCCC(=O)OCc1ccccc1[N+](=O)[O-]
Reaction #744646
2-nitrobenzyl undec-10-enoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_12
O=C(CCCCCCCCCCBr)OCc1ccccc1[N+](=O)[O-]
Reaction #744647
2-nitrobenzyl 11-bromoundecanoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_12
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